<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
AbbVie Data Science is the best-in-class team within its cross-industry peer group and is responsible for bringing people, process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and innovation. This role is key to ensuring successful delivery against the program and maintaining best in industry resources.
 Responsibilities:&nbsp;
<ul>
<li>Manage multiple TA</li>
<li>Manage technology evaluations and implementations for performance improvement and cost reduction.</li>
<li>Creates and sustains an environment that attracts, develops and retains strong talent.</li>
<li>Practice continuous improvement of processes and technology usage.</li>
<li>Acts as subject matter expert and process owner.</li>
<li>Supervises and allocates internal and external resources within the Therapeutic Area.</li>
<li>Ensure all performance assessment responsibilities are achieved for direct reports. Provide training and feedback, resolve personnel issues, and manage talent retention for assigned staff.</li>
<li>Responsible for the performance management of staff; supporting team in building and maintaining a high performing team, recruitment, onboarding, resource assignment, and development opportunities for staff within responsibility.</li>
<li>Manage cross functional initiatives.</li>
<li>Provides strategic direction, advice and guidance to staff in relation to operations responsibilities andactivities; promotes best practice; ensures objectives are successfully met.</li>
</ul>
*This is a US remote position&nbsp;
Qualifications 
<ul>
<li>Bachelor’s degree in management information systems, computer science, life sciences or equivalent.</li>
<li>Master’s preferred.</li>
<li>Must have 8+ years of experience with clinical database design, data loading, and database modeling concepts or 9+ years of experience in a similar technical or clinical development environment.</li>
<li>Demonstrated intermediate SAS and/or SQL programming skills and expert knowledge of database concepts.</li>
<li>In-depth knowledge of CDASH and SDTM Standards In-depth understanding of clinical trial processes</li>
<li>Demonstrated ability to influence others without direct authority. Demonstrated performance as a key contributor to initiatives and advancement of the organization. Demonstrated ability to successfully coach/mentor in a matrix environment Demonstrated effective communication skills Demonstrated effective analytical skills</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Manager, Clinical Data Systems (REMOTE)

<h3>Job Description</h3>
Job DescriptionCompany Description 
Glycomine is a small clinical stage bio tech company committed to developing therapeutics for&nbsp; congenital disorders of glycosylation (CDG), serious rare diseases for which the vast majority of which do not have any disease-modifying treatment options available.&nbsp;Many of these diseases are driven by a genetic mutation that disrupts the function of an important enzyme. Glycomine’s lead clinical program in PMM2-CDG aims to deliver a substrate to bypass the enzymatic problem.&nbsp;
Our team has a special dedication to find solutions to the significant unmet medical need experienced by patients and families with rare diseases. We come from many disciplines and bring multiple viewpoints and broad expertise to our mission. We are driven by the imperative and the opportunity to develop therapies that can provide meaningful improvements in the quality of life for patients, caregivers, and families.
Job Description 
The Senior Clinical Project Manager/Clinical Project Manager is a team-player role responsible for supporting aspects of clinical operations for our programs. This individual possesses clinical operations expertise with a track record of success, working with peers and stakeholders across multiple disciplines to drive a key program with multiple studies and indications through all phases of clinical trials (Phase I-III). The Senior Clinical Project Manager/Clinical Project Manager is a role in the Clinical Development organization who knows how to work closely with vendors and clinical sites.
As a Senior Clinical Project Manager/Clinical Project Manager at Glycomine, you will play a pivotal role in driving the success of critical clinical programs. You'll provide support and experience to the program and members of our Clinical Development team to ensure the seamless execution of clinical trials. In this role, you'll collaborate across diverse functions, support key initiatives, and promote timely, on-budget trial completion that adheres to the highest quality standards.
You will be a member of a team that is responsible for the planning, implementation, execution, and management of clinical studies by overseeing day-to-day operations and directly managing and working with outside Clinical Research Organizations (CROs), clinical sites and their teams, and third-party vendors. You will thrive in a fast-paced, innovative environment, while remaining flexible, proactive, resourceful, and efficient. The ability to analyze complex issues to quickly develop relevant and realistic plans and recommendations for implementation is essential. Also necessary are excellent matrix management skills, written and verbal communication skills, attention to detail, and knowledge of quality obligations.
This is a remote based position ideally located in east coast time zone. Responsibilities include, but are not limited to the following:
<ul>
<li>Prepare or review site feasibility reports and support the study team in site selection.</li>
<li>Ensure efficient and through study start-up, by overseeing the CRO and vendors and working closely with relevant team members involved in study set up (CMC, Reg, etc). Ensure timeline collection of all start-up documents (example ethics documents for submission), site Clinical Trial Agreements and start up activities are performed prior to each site activation.</li>
<li>Work closely with the Director of Clinical Operations to review the study timelines and milestones are being met.</li>
<li>Manage the scope of work, change notifications, contract modification, site trial agreements, and other necessary budgetary information for clinical trial operations</li>
<li>Review site visits per Oversight Plan and conduct study oversights as needed.</li>
<li>Be responsible for oversight activities of vendors (example CRO, lab vendors, etc)</li>
<li>Assist in the preparation and implementation of study plans (example Monitoring Plan, Oversight Plan, etc).</li>
<li>Collaborate cross functionally with internal teams, including Clinical Development, Regulatory Affairs, Translational Medicine and Program Leadership to ensure alignment on clinical trial objectives and milestones</li>
<li>Serve as a point of contact for CROs and vendors, overseeing their performance and ensuring adherence to contractual agreements, timelines and quality standards</li>
<li>Ensure compliance with regulatory requirements, ICH-GCP requirements, and company SOPs throughout all stages of clinical trial conduct</li>
<li>Oversee the collection, analysis and interpretation of clinical trial data, working closely with Clinical Development, Biostatistics and Data Management teams to ensure data accuracy and integrity</li>
<li>Contribute, if needed, to the preparation and review of clinical study documents including the Investigator Brochure, Investigational New Drug Applications (IND), study protocols, clinical study reports, applicable sections of New Drug Applications (NDA) and or Marketing Authorization Application (MAA), updates to the IND, NDA and other safety reports.</li>
<li>Forge strong relationships with investigators, site staff, and CROs, effectively communicating study concepts while overseeing operational strategies for achieving program goals.</li>
<li>&nbsp;Contribute in review of operational risk management strategies</li>
<li>&nbsp;Part of the team who oversee the timely capture, reporting, and evaluation of adverse events and product safety issues.</li>
<li>Oversee clinical and regulatory files, including the essential Trial Master File (TMF).</li>
<li>Work cross-functionally to support the relevant and timely exchange of information and materials to support clinical trial deliverables</li>
<li>Be part of the team that manages clinical trials from start-up through close-out to ensure that both internal and external deliverables are on time and on budget while collaborating across functional areas</li>
<li>Proactively manage clinical trial outsourced partners, including identification of risk, to ensure trial deliverables and performance goals are met</li>
<li>Maintain partnerships through positive relationships with CRO counterparts; proactively review and identify potential issues or problems with the sites and communicate/escalate to clinical leadership</li>
<li>Collaborate with CROs to keep the clinical study database current, accurate, and routinely cleaned</li>
<li>Support and manage oversight activities of all necessary vendors to ensure a high level of operational excellence is maintained</li>
</ul>
Qualifications 
Qualifications:
<ul>
<li>BA/BS preferably in a health-related field; preferred MA/MS degree in biological, life science, nursing or related field but not required.</li>
<li>At least 5 years of experience in clinical operations within the pharmaceutical or biotechnology industry.</li>
<li>Strong experience in managing and developing relationships with contract research organizations (CROs).</li>
<li>Demonstrated excellence in managing clinical trials and a solid understanding of the trial processes.</li>
<li>Proven track record of success and a history of innovative program and trial execution to ensure study progress, timelines, data integrity, and compliance with health authority requirements.</li>
<li>Domain expertise in drug development, with a preference for experience in early-stage clinical trials.</li>
<li>Strong vendor and project management skills are critical.</li>
<li>Ability to manage multiple competing priorities and adapt to changes.</li>
<li>Strong communication, interpersonal, and problem solving skills.</li>
<li>Must be comfortable working in a fast-paced environment.</li>
<li>Global studies (multiple countries and sites) experience required.</li>
<li>Previous experience in the pediatric trials and rare disease is an asset.</li>
<li>Able to work in a team and within a multi-disciplinary environment.</li>
<li>Strong working knowledge of GCP/ICH and other applicable regulations/guidelines, required</li>
<li>Proactive approach</li>
<li>Languages: Strong written and verbal English required.</li>
<li>Travel Requirements: Domestic or internation travel may be required. The position is remote based, though travel will be necessary prerequisite in order to support the program.</li>
</ul>
 Additional Information 
All your information will be kept confidential according to EEO guidelines.

Senior Clinical Project Manager/Clinical Project Manager (Remote)

<h3>Job Description</h3>
Job DescriptionCompany Description 
Company Overview
Glycomine is a small clinical stage bio tech company committed to developing therapeutics for[RM1]&nbsp; congenital disorders of glycosylation (CDG), serious rare diseases for which the vast majority of which do not have any disease-modifying treatment options available.&nbsp;Many of these diseases are driven by a genetic mutation that disrupts the function of an important enzyme. Glycomine’s lead clinical program in PMM2-CDG aims to deliver a substrate to bypass the enzymatic problem.&nbsp;
Our team has a special dedication to find solutions to the significant unmet medical need experienced by patients and families with rare diseases. We come from many disciplines and bring multiple viewpoints and broad expertise to our mission. We are driven by the imperative and the opportunity to develop therapies that can provide meaningful improvements in the quality of life for patients, caregivers, and families.
Job Description 
Role Overview
The Clinical Project Manager is a team-player role responsible for supporting aspects of clinical operations for our programs. This individual possesses clinical operations expertise with a track record of success, working with peers and stakeholders across multiple disciplines to drive a key program with multiple studies and indications through all phases of clinical trials (Phase I-III). The Clinical Project Manager is a role in the Clinical Development organization who knows how to work closely with vendors and clinical sites.
As a Clinical Project Manager at Glycomine, you will play a pivotal role in driving the success of critical clinical programs. You'll provide support and experience to the program and members of our Clinical Development team to ensure the seamless execution of clinical trials. In this role, you'll collaborate across diverse functions, support key initiatives, and promote timely, on-budget trial completion that adheres to the highest quality standards.
You will be a member of a team that is responsible for the planning, implementation, execution, and management of clinical studies by overseeing day-to-day operations and directly managing and working with outside Clinical Research Organizations (CROs), clinical sites and their teams, and third-party vendors. You will thrive in a fast-paced, innovative environment, while remaining flexible, proactive, resourceful, and efficient. The ability to analyze complex issues to quickly develop relevant and realistic plans and recommendations for implementation is essential. Also necessary are excellent matrix management skills, written and verbal communication skills, attention to detail, and knowledge of quality obligations. Responsibilities
<ul>
<li>Prepare or review site feasibility reports and support the study team in site selection.</li>
<li>Ensure efficient and through study start-up, by overseeing the CRO and vendors and working closely with relevant team members involved in study set up (CMC, Reg, etc). Ensure timeline collection of all start-up documents (example ethics documents for submission), site Clinical Trial Agreements and start up activities are performed prior to each site activation.</li>
<li>Assist the Director of Clinical Operations to review the study timelines and milestones are being met.</li>
<li>Review site visits per Oversight Plan and conduct study oversights as needed.</li>
<li>Responsible for oversight activities of vendors (example CRO, lab vendors, etc)</li>
<li>Assist in the preparation and implementation of study plans (example Monitoring Plan, Oversight Plan, etc).</li>
<li>Collaborate cross functionally with internal teams, including Clinical Development, Regulatory Affairs, Translational Medicine and Program Leadership to ensure alignment on clinical trial objectives and milestones</li>
<li>Serve as a point of contact for CROs and vendors, overseeing their performance and ensuring adherence to contractual agreements, timelines and quality standards</li>
<li>Ensure compliance with regulatory requirements, ICH-GCP requirements, and company SOPs throughout all stages of clinical trial conduct</li>
<li>Oversee the collection, analysis and interpretation of clinical trial data, working closely with Clinical Development, Biostatistics and Data Management teams to ensure data accuracy and integrity</li>
<li>Contribute, if needed, to the preparation and review of clinical study documents including the Investigator Brochure, Investigational New Drug Applications (IND), study protocols, clinical study reports, applicable sections of New Drug Applications (NDA) and or Marketing Authorization Application (MAA), updates to the IND, NDA and other safety reports.</li>
<li>Forge strong relationships with investigators, site staff, and CROs, effectively communicating study concepts while overseeing operational strategies for achieving program goals.</li>
<li>&nbsp;Contribute in review of operational risk management strategies</li>
<li>&nbsp;Part of the team who oversee the timely capture, reporting, and evaluation of adverse events and product safety issues.</li>
<li>Oversee clinical and regulatory files including the essential Trial Master File (TMF).</li>
<li>Be part of the team that manages clinical trials from start-up through close-out to ensure that both internal and external deliverables are on time and on budget while collaborating across functional areas</li>
<li>Proactively manage clinical trial outsourced partners, including identification of risk, to ensure trial deliverables and performance goals are met</li>
<li>Maintain partnerships through positive relationships with CRO counterparts; proactively review and identify potential issues or problems with the sites and communicate/escalate to clinical leadership</li>
<li>Collaborate with CROs to keep the clinical study database current, accurate, and routinely cleaned</li>
<li>Support and manage oversight activities of all necessary vendors to ensure a high level of operational excellence is maintained</li>
</ul>
Qualifications 
<ul>
<li>BA/BS preferably in a health-related field; preferred MA/MS degree in biological, life science, nursing or related field but not required.</li>
<li>At least 5 years of experience in clinical operations within the pharmaceutical or biotechnology industry.</li>
<li>Strong experience in managing and developing relationships with contract research organizations (CROs).</li>
<li>Demonstrated excellence in managing clinical trials and a solid understanding of the trial processes.</li>
<li>Proven track record of success and a history of innovative program and trial execution to ensure study progress, timelines, data integrity, and compliance with health authority requirements.</li>
<li>Domain expertise in drug development, with a preference for experience in early-stage clinical trials.</li>
<li>Strong vendor and project management skills are critical.</li>
<li>Ability to manage multiple competing priorities and adapt to changes.</li>
<li>Global studies (multiple countries and sites) experience required.</li>
<li>Previous experience in the pediatric trials and rare disease is a plus.</li>
<li>Strong working knowledge of GCP/ICH and other applicable regulations/guidelines, required</li>
<li>Travel Requirements: Remote role requiring up to 25% travel</li>
</ul>
 Additional Information 
All your information will be kept confidential according to EEO guidelines.

Clinical Project Manager (Remote)

<h3>Job Description</h3>
Job Description
We are looking for a Clinical Trials Project Manager II to join our team!
APPLY DIRECTLY at <a href="https://cpcclinicalresearch.org/careers/" target="_blank">https://cpcclinicalresearch.org/careers/</a> (internal title Clinical Operations Manager II)
Are you well organized, but adaptable to unexpected changes? Someone who is able to see the bigger picture, without losing sight of the day-to-day tasks? If the answer is yes, keep reading!
This role serves as the primary point of contact for industry sponsored clinical trials and Endpoint and Specialty Services activities.
In this position you will:
<ul>
<li>Oversee clinical operations management activities</li>
<li>Define and monitor project scope, timelines and deliverables from project initiation to close-out.</li>
<li>Identify project-specific training for team members and notify appropriate designee to ensure completion and filing of training documentation.</li>
<li>Oversee trial-related activities.</li>
<li>Track and approve vendor payments.</li>
<li>Provide expert advice in the design, writing and/or review of all project-related essential documents including protocols, project management plans, case report forms, statistical analysis plans, project management plans, ICF templates, study procedure manuals, source documents, site newsletters, study reports, resource tools, essential documents, monitoring plans and report templates.</li>
<li>Develop and manage multidisciplinary project team members. Organize, plan for, and produce minutes for project team meetings.</li>
<li>Ensure the overall quality of project services and deliverables.</li>
<li>Provide necessary updates and reports to the sponsor as outlined by the contract.</li>
<li>Plan and oversee the execution of investigator meetings as contracted.</li>
<li>Work with the Business Development team on budgets, proposals and change orders.</li>
<li>Ensure both CPC and sponsor are aware of and in agreement on any change in project scope that has a financial or resource impact.</li>
<li>Provide Head of Trial Master File scope of services to enable him/her to establish and maintain Trial Master Files (TMFs) and project document files, both electronic and paper.</li>
<li>Adhere to local, federal and international regulations, guidelines and CPC Policies, Standard Operating Procedures (SOPs) and Work Instructions (WIs). Use appropriate discretion to proactively identify when there is a need to deviate from policies, procedures or plans and ensure deviations are appropriately documented.</li>
<li>Define and monitor Endpoint and Specialty Services scope, timelines and deliverables from project initiation to closeout with assistance from study assigned Clinical Operations Manager and the Head of Endpoint and Specialty Services.</li>
<li>Manage contracted deliverables for external committees (e.g. data safety monitoring boards, clinical endpoint committees), including but not limited to meeting scheduling, generation of meeting minutes and distribution of meeting materials.</li>
<li>Oversee SAE process and assure execution of safety plans.</li>
<li>Accurately track receipt, entry, upload and the processing of photos, acetate tracings, and other source documents submitted from sites.</li>
<li>Contact appropriate individuals (e.g., study site staff or study site Clinical Research Associate) regarding incomplete, inaccurate, or missing photos, acetate tracings, and other Endpoint and Specialty Services Core Lab documents as required by the project.</li>
<li>Oversee timely and accurate entry and cleaning of data for all study databases; maintain and file data management documentation as required.</li>
<li>Provide feedback to study sites on tracing and quality issues, as required by project.</li>
<li>Manage and conduct Endpoint and Specialty Services CPC Core Lab activities.</li>
<li>Provide operational support for the biostatistics and programming deliverables.</li>
</ul>
Here’s what you will need to bring to the table:
<ul>
<li>Nursing or BA/BS in a scientific field (or equivalent knowledge/experience).</li>
<li>4 years of experience in a clinical research setting, including a minimum of 2 years of project/operations management experience in clinical research (required).</li>
<li>Demonstrated ability to adequately manage all facets of a clinical trial with minimal direction.</li>
<li>Thorough knowledge of the Good Clinical Practice guidelines and applicable FDA and ICH regulations for conducting clinical drug trials.</li>
<li>Proficiency in Microsoft Office, particularly Outlook, Word and Excel.</li>
<li>Excellent communication and organizational skills.</li>
<li>Great attention to detail.</li>
<li>Exemplary skills leading and managing multi-disciplinary teams in a clinical research setting.</li>
<li>Ability to organize, instruct and oversee project staff, while promoting group effort and achievement.</li>
<li>Ability to adapt quickly to new situations, manage conflicts and resolve problems effectively.</li>
<li>Willingness to travel 20-25%.</li>
</ul>
Note: Viable applicants will be required to pass a background and education verification check.
Targeted Compensation: $72,000 – $95,000 annually
Company DescriptionAbout CPC: CPC is an academic research organization that offers full service clinical trial design, oversight, and management with rapid access to Key Opinion Leaders in a variety of therapeutic areas. With over 35 years of experience, CPC has provided services to over 150 clinical trials in a variety of indications, with an emphasis on cardiovascular, wound healing, diabetes and more. CPC has expertise in managing clinical trials from a variety of funding sources including Industry, NIH, and Investigator Initiated trials. CPC Community Health focuses on innovative programs that reach into communities to help people find effective ways to become active, empowered and healthy. <a href="http://www.cpccommunityhealth.org/" target="_blank">http://www.cpccommunityhealth.org/</a> CPC offers: * Comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.) * Matching 401(k) plan (dollar for dollar up to 4% of your eligible compensation, fully vested immediately) * 11 paid holidays * 15 - 25 vacation days based on years of service * Paid sick time (2.67 hours accrued bi-weekly up to a maximum of 80 hours) * Monthly fun events (e.g. team building activities, games, charitable events, potlucks, picnics) * Flexible and remote work schedules available for certain positions Visit our web site to learn more about us and values we embrace: <a href="https://cpcclinicalresearch.org/" target="_blank">https://cpcclinicalresearch.org/</a>. An Equal Opportunity Employer CPC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race (including traits historically associated with race, such as hair texture and length, protective hairstyles), sex, color, ancestry, sexual orientation, gender identity, gender expression, marital status, religion, creed, national origin, disability, military status, genetic information, age 40 and over or any other status protected by applicable federal, state or local law. It is our intention that all qualified applicants are given equal opportunity and that selection decisions be based on job-related factors. Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act (ADA) and certain state or local laws. If you need assistance, please email our Human Resources team at <a href="mailto:careers@cpcmed.org" target="_blank">careers@cpcmed.org</a>. 
<h3>Company Description</h3>
About CPC:\r\nCPC is an academic research organization that offers full service clinical trial design, oversight, and management with rapid access to Key Opinion Leaders in a variety of therapeutic areas. With over 35 years of experience, CPC has provided services to over 150 clinical trials in a variety of indications, with an emphasis on cardiovascular, wound healing, diabetes and more. \r\n\r\nCPC has expertise in managing clinical trials from a variety of funding sources including Industry, NIH, and Investigator Initiated trials.\r\n\r\nCPC Community Health focuses on innovative programs that reach into communities to help people find effective ways to become active, empowered and healthy. <a href="http://www.cpccommunityhealth.org/" target="_blank">http://www.cpccommunityhealth.org/</a> \r\n\r\nCPC offers:\r\n* Comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.)\r\n* Matching 401(k) plan (dollar for dollar up to 4% of your eligible compensation, fully vested immediately)\r\n* 11 paid holidays\r\n* 15 - 25 vacation days based on years of service\r\n* Paid sick time (2.67 hours accrued bi-weekly up to a maximum of 80 hours) \r\n* Monthly fun events (e.g. team building activities, games, charitable events, potlucks, picnics)\r\n* Flexible and remote work schedules available for certain positions\r\n\r\nVisit our web site to learn more about us and values we embrace: <a href="https://cpcclinicalresearch.org/" target="_blank">https://cpcclinicalresearch.org/</a>.\r\n\r\nAn Equal Opportunity Employer\r\nCPC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race (including traits historically associated with race, such as hair texture and length, protective hairstyles), sex, color, ancestry, sexual orientation, gender identity, gender expression, marital status, religion, creed, national origin, disability, military status, genetic information, age 40 and over or any other status protected by applicable federal, state or local law. It is our intention that all qualified applicants are given equal opportunity and that selection decisions be based on job-related factors.\r\n\r\nApplicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act (ADA) and certain state or local laws. If you need assistance, please email our Human Resources team at <a href="mailto:careers@cpcmed.org" target="_blank">careers@cpcmed.org</a>.

Clinical Trials Project Manager II - remote

<h3>Job Description</h3>
Job Description
Clinical Trial Manager
Come Join the DCN Dx team!
As Clinical Trial Manager, you will work with our clients to deliver clinical research support, from initial clinical and regulatory strategy through to the final clinical study report. Ideally, you'll have over 7 years of experience working in clinical research, clinical affairs or clinical operations, with significant IVD experience. This position will be remote, full-time reporting to the Vice President of Clinical Research.
Essential Functions
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
<ol>
<li>Work with the Clinical Research team to oversee clinical sites and manage clinical trials on behalf of DCN Dx clients.</li>
<li>Write clinical trial-specific documents including but not limited to: protocols, case report forms, case report form completion guidelines, monitoring plan, source worksheets, specimen management plans and Study Manual of Operations</li>
<li>Lead identification, qualification, initiation, monitoring and closeout of clinical trial sites</li>
<li>Manage inventory of investigational product and ensure sites are properly supplied</li>
<li>Review clinical data for accuracy and raise queries as needed</li>
<li>Work with Data Management and Biostatistics to ensure timely receipt, review and completion of data for clinical databases</li>
<li>Manage, track, and report all protocol deviations </li>
<li>Perform other tasks and duties as assigned.</li>
<li>Develop SOPs for Clinical Research</li>
<li>Effectively utilizes external resources to meet project objectives.</li>
<li>Demonstrates and advocates the DCN Dx Culture of customer service and excellence.</li>
</ol>
Travel
Ability to travel up to 50%.
Required Education and Experience
<ol>
<li>BS or BA in biology or biochemistry or a related field or BS/BA in another field with at least 10 years of experience in Clinical Research</li>
<li>7+ years of experience managing clinical trials, IVD experience preferred</li>
<li>Strong understanding of GCP/ICH requirements, with an emphasis on US clinical trials management</li>
<li>Strong consulting skills, excellent oral and written communications and interpersonal skills. Ability to work in teams is critical. Basic knowledge of MS Office products and familiarity with data collection tools a must.</li>
</ol>
Knowledge and Skills
<ol>
<li>FDA regulations, GMP/GLP/GCP &amp; Lean Manufacturing</li>
<li>Full proficiency with various laboratory techniques/instruments</li>
<li>Thorough knowledge of applicable safety and standards guidelines, such as FDA, SOP, cGMP, regulations, and/or MSDS</li>
<li>Demonstrated competence in conducting chemical analyses</li>
<li>Strong knowledge of wet chemistry techniques</li>
<li>Ability to critically review and analyze data, interpret information, and draw conclusions from relevant or missing information.</li>
<li>Strong verbal and written communication skills as well as good computer skills</li>
<li>Establish and maintain cooperative working relationships with others.</li>
</ol>
Benefits
<ol>
<li>Medical, Dental, Vision</li>
<li>Life/AD&amp;D, Short-Term Disability, Long-Term Disability</li>
<li>Paid Time Off, Holiday Pay, Maternity/Paternity Leave</li>
<li>401k, 3% Contribution</li>
<li>Amazing Colleagues and Culture</li>
</ol>
AAP/EEO Statement DCN Diagnostics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Clinical Trials Manager

<h3>Job Description</h3>
Job Description
This is a remote position.
The Clinical Project Manager (CPM) is responsible for leading and managing all aspects of clinical trials from initiation through closeout. This includes ensuring that clinical projects are conducted in compliance with applicable regulatory requirements, company SOPs, timelines, and budget. The CPM will serve as the primary point of contact for cross-functional teams, vendors, and sponsors (if applicable), ensuring streamlined communication and timely issue resolution throughout the project lifecycle. Key Responsibilities: Develop, manage, and oversee clinical trial project plans including timelines, milestones, budgets, and resource allocation. Serve as the primary liaison between internal teams, clinical research sites, CROs, vendors, and external partners. Lead cross-functional team meetings and coordinate study activities such as site selection, study start-up, monitoring, and close-out. Ensure adherence to GCP, ICH guidelines, regulatory standards, and company SOPs throughout study conduct. Monitor progress against timelines and budget; proactively identify risks and implement mitigation strategies. Oversee vendor performance and manage contract deliverables for CROs, central labs, data management providers, etc. Track clinical trial metrics and prepare regular status reports for internal leadership and/or sponsors. Support regulatory and audit readiness, including contributing to study documentation and inspection preparation. Participate in protocol development, CRF design, and review of key trial documents (e.g., ICF, SAP, CSR). Minimum Qualifications: Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field (Master’s or PMP certification a plus). Minimum of 5 years of experience in clinical research, including 2+ years in a project management role. Strong understanding of GCP, ICH guidelines, and clinical trial regulatory requirements. Proven ability to manage multi-site and/or global studies across various phases (Phase I–IV). Excellent organizational, problem-solving, and leadership skills. Strong interpersonal and written communication skills. Proficiency with clinical trial management systems (CTMS), MS Project, and Microsoft Office Suite. In addition to a dynamic and collaborative work environment, we offer a comprehensive benefits package to support our employees' well-being. Our benefits include paid holidays, Paid Time Off (PTO) policy, and medical insurance to ensure our team members have the flexibility and coverage they need. We believe in fostering a healthy work-life balance while providing the necessary support for professional and personal growth. E-Verify Participation: Pharmavise Consulting Corporation participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, Pharmavise is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue. For more information on E-Verify, please contact DHS at 888-897-7781 or through their website at dhs.gov/e-verify.

Clinical Project Manager

<h3>Job Description</h3>
Job Description
Clinical Data Manager
This position is based in St. Louis, Missouri, with a hybrid onsite and remote work schedule at the Geneoscopy office.
The Clinical Trial Data Manager is responsible for managing clinical data to support regulatory submissions and product development. This role ensures the accuracy, integrity, and quality of clinical data in compliance with Good Clinical Practice (GCP) and applicable regulatory guidelines.
 
RESPONSIBILITIES
<ul>
<li>Design, review, and approve essential documents and databases, including informed consent forms (ICFs), case report forms (CRFs), and study protocols.</li>
<li>Collaborate with cross-functional teams to define data collection strategies.</li>
<li>Develop and maintain Data Management Plans (DMPs).</li>
<li>Liaise with external partners and internal teams to ensure data integrity and timely delivery.</li>
<li>Monitor data entry for consistency, completeness, and compliance with study protocols.</li>
<li>Implement appropriate systems, standards, and processes to maintain clinical study files per applicable guidance.</li>
<li>Ensure that trials are conducted in compliance with applicable regulations and internal policies, and procedures.</li>
<li>Provide regular updates on study progress to senior leadership and other stakeholders; proactively identify and resolve issues that arise during study conduct; and manage the escalation of study-related issues.</li>
<li>Oversee the clinical aspects of timely data cleaning, data analysis, and the availability of top-line results, participate in data reviews, and review statistical analysis plans.</li>
<li>Author, edit, and/or review written summaries of data reports, presentations, training material, and study documents.</li>
<li>Coordinate with Quality Assurance to ensure internal and external study team members are trained on the appropriate policies and procedures.</li>
<li>Prepare clinical trial reports, regulatory submissions, and support audits or inspections as needed.</li>
<li>Participate in audits and inspections as needed.</li>
<li>Manage and develop a team of Clinical Research Associates (CRAs).</li>
<li>Other duties as assigned.</li>
</ul>
 
EDUCATION REQUIREMENTS
<ul>
<li>Bachelor's degree in Life Sciences, or related field.
<ul>
<li>Master's degree preferred.</li>
</ul>
</li>
</ul>
 
QUALIFICATIONS
<ul>
<li>Possess 5+ years of experience in clinical data management, preferably within a CRO, pharmaceutical, or biotech environment.</li>
<li>Exemplify thorough knowledge of applicable regulations.</li>
<li>Possess strong experience with the management of CROs and other vendors.</li>
<li>Demonstrate strong knowledge of protocol, processes, clinical study design, study planning and management, and monitoring.</li>
<li>Possess the ability to solve complex problems, apply judgment, and make clear recommendations.</li>
<li>Exemplify the ability to multitask and thrive in an agile, fast-paced, deadline-driven environment while remaining flexible, proactive, resourceful, and efficient.</li>
<li>Possess proficient verbal and written communication skills, while willing to share and receive information and ideas from all levels of the organization to achieve the desired results.</li>
<li>Possess high ethics and conduct business in the most professional manner.</li>
<li>Seek inclusiveness and collaboration but step up to responsibility, make tough decisions, and be accountable for those decisions.</li>
<li>Act as a results-oriented team player with strong interpersonal and communication skills, capable of working collaboratively with colleagues.</li>
</ul>
 
SCHEDULE This is a salaried position, requiring at least 40 hours per week. There may be projects that require activities beyond the standard hours.
This role will require travel up to 25%.
 
COMPENSATION &amp; BENEFITS
<ul>
<li>Base salary range: $130,000 - 150,000/annually determined based on the candidate's experience, knowledge, and abilities.</li>
<li>Bonus: discretionary annual bonus based on a percentage of the employee's base salary</li>
<li>Benefits: health, vision, dental, life insurance, 401k (with employer match), and paid time off.</li>
<li>Company Stock Options</li>
</ul>
 
ADDITIONAL INFORMATION
Geneoscopy's Core Values Ability to embody Geneoscopy's beliefs, philosophies, and principles:
<ul>
<li>Integrity - we do the right thing through our words, actions, and behaviors</li>
<li>Courage - step up, speak up, stand out</li>
<li>Agility - think and act fast, embracing change</li>
<li>Passion - for our customers, our people, our work, and for excellence</li>
<li>Collaboration - our differences are assets</li>
</ul>
 Physical Demands
<ul>
<li>Employees may be required to lift routine office supplies and use standard office equipment.</li>
<li>Must possess the ability to sit and/or stand for long periods.</li>
<li>Must possess the ability to perform repetitive motion.</li>
</ul>
 Work Environment
<ul>
<li>May have exposure to fumes and bio-hazardous material in the laboratory environment.</li>
<li>May be required to handle blood-borne pathogens and general laboratory reagents.</li>
</ul>
 
By completing this online employment application, you certify that the information on this application is true and complete to the best of your knowledge. You understand that any misrepresentation or omission of fact in response to any inquiry made in this application may result in the rejection of the application or if hired, dismissal whenever it is discovered. You authorize and release all parties from any liability or damage that may result from seeking, furnishing, or using such information. You understand and agree that, if hired, your employment is for no definite period and may, regardless of the date of payment of compensation, be terminated by Geneoscopy at any time, for any or no reason, with or without notice. You understand that no representation to the contrary is valid unless in writing, setting a definite term of employment, and signed by the company's CEO. You further understand and agree that any job offer is contingent upon your passing, to the company's satisfaction, a criminal background check, reference checks, and other possible screenings. You understand that this application is active for 90 days only, and if you do not hear from the company but still wish to be considered for employment after 90 days, you will need to fill out a new application.

Clinical Data Manager

<h3>Job Description</h3>
Job Description
This is a remote position.
The Clinical Research Manager (CRM) is responsible for the strategic and operational oversight of clinical trials conducted across various phases. This role ensures that studies are executed in compliance with regulatory requirements, GCP/ICH guidelines, and internal SOPs. The CRM manages cross-functional teams, monitors timelines and budgets, and acts as the primary liaison between investigators, CROs, vendors, and internal stakeholders. Key Responsibilities: Lead the planning, execution, and management of clinical trials across multiple therapeutic areas and phases. Oversee site selection, study start-up, patient recruitment, data collection, and close-out activities. Ensure compliance with FDA, ICH-GCP, and other applicable regulatory standards. Develop and maintain project timelines, budgets, and resource plans. Supervise and mentor Clinical Research Associates (CRAs), Clinical Trial Assistants (CTAs), and study coordinators. Review and approve study documentation including protocols, CRFs, informed consent forms, and monitoring reports. Coordinate with cross-functional teams including regulatory affairs, data management, biostatistics, and medical writing. Manage vendor and CRO relationships, including contract negotiations and performance monitoring. Track and report on study metrics and provide regular updates to senior leadership. Oversee the preparation and conduct of audits and regulatory inspections. Minimum Qualifications: Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field (Master’s or Ph.D. preferred). Minimum of 5–7 years of experience in clinical research, including 2+ years in a managerial or supervisory role. In-depth knowledge of clinical trial processes, ICH-GCP guidelines, and regulatory requirements. Proven experience managing Phase I-IV trials across multiple therapeutic areas. Strong project management, leadership, and team coordination skills. Excellent written and verbal communication abilities. Proficiency with clinical trial software (e.g., CTMS, EDC, eTMF platforms). Ability to travel up to 20% as needed. In addition to a dynamic and collaborative work environment, we offer a comprehensive benefits package to support our employees' well-being. Our benefits include paid holidays, Paid Time Off (PTO) policy, and medical insurance to ensure our team members have the flexibility and coverage they need. We believe in fostering a healthy work-life balance while providing the necessary support for professional and personal growth. 
E-Verify Participation: 
Pharmavise Consulting Corporation participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, Pharmavise is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue. For more information on E-Verify, please contact DHS at 888-897-7781 or through their website at dhs.gov/e-verify.

Clinical Research Manager

<h3>Job Description</h3>
Job Description
Customer Success Manager – Remote (Full-Time)
&nbsp;Location: Remote (US-based preferred) Department: Customer Success / Clinical Trials Reports to: VP of Clinical Trials
Company Overview
Vivalink is a leader in digital health technology, delivering advanced remote data capture solutions for healthcare and clinical research. Our Biometrics Data Platform integrates FDA-cleared medical-grade wearable sensors, cloud-based data services, machine learning algorithms, and clinician software—empowering global organizations to design and deploy remote patient monitoring (RPM) and decentralized clinical trial (DCT) solutions.
We support pharmaceutical companies, CROs, Academia, and healthcare providers with the tools to capture high-quality, real-time physiological data across a wide range of therapeutic areas, including cardiology, neurology, infectious disease, oncology, and rare diseases.
Role Summary
We are seeking a dynamic, detail-oriented Customer Success Manager (CSM) to join our team and help ensure the success of our growing base of clinical research customers. The CSM will serve as the primary point of contact post-sale, responsible for onboarding, project coordination, troubleshooting, relationship development, account penetration, and long-term retention.
You will work closely with cross-functional teams—including Solutions Engineering, Product, Operations, and Sales—to ensure our customers receive an exceptional experience and achieve their desired outcomes.
Key Responsibilities
<ul>
<li>
Customer Onboarding &amp; Implementation &nbsp;
<ul>
<li>
Coordinate the onboarding process for new clinical trials and RPM deployments, including technical setup, workflow design, training, and user enablement.
</li>
<li>
Collaborate with clients to define project goals, success metrics, and timelines. &nbsp;
</li>
</ul>
</li>
<li>
Account Management &amp; Retention &nbsp;
<ul>
<li>
Serve as the trusted advisor and point of contact for assigned customer accounts and as the liaison between customer and internal teams, such as Product, Sales, Operations and Support.
</li>
<li>
Monitor ongoing study health and proactively identify issues, ensuring timely resolution.
</li>
<li>
Drive renewals and expansions by demonstrating value and anticipating customer needs.
</li>
<li>
Be the voice of the customer within the organization to ensure needs are prioritized. &nbsp;
</li>
</ul>
</li>
<li>
Cross-Functional Coordination &nbsp;
<ul>
<li>
Work with Product, Sales, Operations and Support teams to escalate and resolve customer concerns and issues quickly and effectively.
</li>
<li>
Work with finance to support timely collections.
</li>
<li>
Provide customer feedback to inform roadmap priorities and service improvements. &nbsp;
</li>
</ul>
</li>
<li>
Performance Monitoring &amp; Reporting &nbsp;
<ul>
<li>
Track device usage, data quality, participant adherence, and other key performance indicators.
</li>
<li>
Track progress against defined project goals, success metrics, and timelines
</li>
<li>
Deliver regular reports and business reviews with actionable insights. &nbsp;
</li>
</ul>
</li>
<li>
Advocacy &amp; Relationship Building &nbsp;
<ul>
<li>
Cultivate strong relationships with clinical operations, data managers, investigators, and study coordinators.
</li>
<li>
Promote Vivalink’s broader capabilities to drive customer expansion and satisfaction. &nbsp;
</li>
</ul>
</li>
</ul>
Qualifications
Required:
<ul>
<li>
5+ years in a Customer Success, Clinical Operations, Project Management, or related client-facing role.
</li>
<li>
Demonstrates a strong ability to understand, communicate, and create alignment with different stakeholders in the client’s organization
</li>
<li>
Strong understanding of digital health, clinical trials, and remote patient monitoring
</li>
<li>
Strong experience working with pharmaceutical, biotech and CRO companies.
</li>
<li>
Excellent written and verbal communication skills.
</li>
<li>
Analytical mindset with the ability to interpret data and derive insights.
</li>
<li>
Comfortable working in a fast-paced, startup-like environment with minimal supervision.
</li>
<li>
Bachelor's degree in Life Sciences, Healthcare, Business, or related field. &nbsp;
</li>
</ul>
Preferred:
<ul>
<li>
Experience with medical devices, wearables, or remote patient monitoring solutions.
</li>
<li>
Familiarity with clinical trial operations, GCP, ICH guidelines, or regulatory considerations (e.g., HIPAA, 21 CFR Part 11).
</li>
<li>
Experience with digital tools such as Hubspot, Jira, Slack, or Confluence.
</li>
<li>
Clinical research certification (e.g., CCRA, CCRC, PMP) is a plus. &nbsp;
</li>
</ul>
Why Join Vivalink?
<ul>
<li>
Be at the forefront of remote patient monitoring innovation.
</li>
<li>
Work with a collaborative, mission-driven team.
</li>
<li>
Contribute to impactful studies in areas like cardiology, oncology, and infectious diseases.
</li>
<li>
Fully remote and flexible work culture.
</li>
<li>
Competitive salary, equity, and benefits. &nbsp;
</li>
</ul>
Company DescriptionVivalink Campbell, CA Company Silicon Valley-based Vivalink (<a href="http://www.vivalnk.com" target="_blank">www.vivalnk.com</a>) is an innovative connected healthcare devices company in its growth stage. The company develops wearable telemetry devices with integrated biometric sensors designed to continuously monitor human vitals and other indicators for medical and healthcare applications. These devices together with Vivalink’s related healthcare software products and services are offered to enterprise customers under a platform as a service model. Over 300 leading organizations, in more than 50 countries depend on our wearable human vitalssensors, software and services. With great products, more than 20 patents and brilliant people, what we do matters. 
<h3>Company Description</h3>
Vivalink\r\nCampbell, CA\r\nCompany\r\nSilicon Valley-based Vivalink (<a href="http://www.vivalnk.com" target="_blank">www.vivalnk.com</a>) is an innovative connected healthcare devices company in its growth stage. The company develops wearable telemetry devices with integrated biometric sensors designed to continuously monitor human vitals and other indicators for medical and healthcare applications. These devices together with Vivalink’s related healthcare software products and services are offered to enterprise customers under a platform as a service model. Over 300 leading organizations, in more than 50 countries depend on our wearable human vitalssensors, software and services. With great products, more than 20 patents and brilliant people, what we do matters.

Customer Success Manager/Clinical Trials - Remote (Full-Time)

<h3>Job Description</h3>
Job Description
We are looking for a Clinical Trials Project Manager II to join our team!
APPLY DIRECTLY at <a href="https://cpcclinicalresearch.org/careers/" target="_blank">https://cpcclinicalresearch.org/careers/</a> (internal title Clinical Operations Manager II)
Are you well organized, but adaptable to unexpected changes? Someone who is able to see the bigger picture, without losing sight of the day-to-day tasks? If the answer is yes, keep reading!
This role serves as the primary point of contact for industry sponsored clinical trials and Endpoint and Specialty Services activities.
In this position you will:
<ul>
<li>Oversee clinical operations management activities</li>
<li>Define and monitor project scope, timelines and deliverables from project initiation to close-out.</li>
<li>Identify project-specific training for team members and notify appropriate designee to ensure completion and filing of training documentation.</li>
<li>Oversee trial-related activities.</li>
<li>Track and approve vendor payments.</li>
<li>Provide expert advice in the design, writing and/or review of all project-related essential documents including protocols, project management plans, case report forms, statistical analysis plans, project management plans, ICF templates, study procedure manuals, source documents, site newsletters, study reports, resource tools, essential documents, monitoring plans and report templates.</li>
<li>Develop and manage multidisciplinary project team members. Organize, plan for, and produce minutes for project team meetings.</li>
<li>Ensure the overall quality of project services and deliverables.</li>
<li>Provide necessary updates and reports to the sponsor as outlined by the contract.</li>
<li>Plan and oversee the execution of investigator meetings as contracted.</li>
<li>Work with the Business Development team on budgets, proposals and change orders.</li>
<li>Ensure both CPC and sponsor are aware of and in agreement on any change in project scope that has a financial or resource impact.</li>
<li>Provide Head of Trial Master File scope of services to enable him/her to establish and maintain Trial Master Files (TMFs) and project document files, both electronic and paper.</li>
<li>Adhere to local, federal and international regulations, guidelines and CPC Policies, Standard Operating Procedures (SOPs) and Work Instructions (WIs). Use appropriate discretion to proactively identify when there is a need to deviate from policies, procedures or plans and ensure deviations are appropriately documented.</li>
<li>Define and monitor Endpoint and Specialty Services scope, timelines and deliverables from project initiation to closeout with assistance from study assigned Clinical Operations Manager and the Head of Endpoint and Specialty Services.</li>
<li>Manage contracted deliverables for external committees (e.g. data safety monitoring boards, clinical endpoint committees), including but not limited to meeting scheduling, generation of meeting minutes and distribution of meeting materials.</li>
<li>Oversee SAE process and assure execution of safety plans.</li>
<li>Accurately track receipt, entry, upload and the processing of photos, acetate tracings, and other source documents submitted from sites.</li>
<li>Contact appropriate individuals (e.g., study site staff or study site Clinical Research Associate) regarding incomplete, inaccurate, or missing photos, acetate tracings, and other Endpoint and Specialty Services Core Lab documents as required by the project.</li>
<li>Oversee timely and accurate entry and cleaning of data for all study databases; maintain and file data management documentation as required.</li>
<li>Provide feedback to study sites on tracing and quality issues, as required by project.</li>
<li>Manage and conduct Endpoint and Specialty Services CPC Core Lab activities.</li>
<li>Provide operational support for the biostatistics and programming deliverables.</li>
</ul>
Here’s what you will need to bring to the table:
<ul>
<li>Nursing or BA/BS in a scientific field (or equivalent knowledge/experience).</li>
<li>4 years of experience in a clinical research setting, including a minimum of 2 years of project/operations management experience in clinical research (required).</li>
<li>Demonstrated ability to adequately manage all facets of a clinical trial with minimal direction.</li>
<li>Thorough knowledge of the Good Clinical Practice guidelines and applicable FDA and ICH regulations for conducting clinical drug trials.</li>
<li>Proficiency in Microsoft Office, particularly Outlook, Word and Excel.</li>
<li>Excellent communication and organizational skills.</li>
<li>Great attention to detail.</li>
<li>Exemplary skills leading and managing multi-disciplinary teams in a clinical research setting.</li>
<li>Ability to organize, instruct and oversee project staff, while promoting group effort and achievement.</li>
<li>Ability to adapt quickly to new situations, manage conflicts and resolve problems effectively.</li>
<li>Willingness to travel 20-25%.</li>
</ul>
Note: Viable applicants will be required to pass a background and education verification check.
Targeted Compensation: $72,000 – $95,000 annually
Company DescriptionAbout CPC: CPC is an academic research organization that offers full service clinical trial design, oversight, and management with rapid access to Key Opinion Leaders in a variety of therapeutic areas. With over 35 years of experience, CPC has provided services to over 150 clinical trials in a variety of indications, with an emphasis on cardiovascular, wound healing, diabetes and more. CPC has expertise in managing clinical trials from a variety of funding sources including Industry, NIH, and Investigator Initiated trials. CPC Community Health focuses on innovative programs that reach into communities to help people find effective ways to become active, empowered and healthy. <a href="http://www.cpccommunityhealth.org/" target="_blank">http://www.cpccommunityhealth.org/</a> CPC offers: * Comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.) * Matching 401(k) plan (dollar for dollar up to 4% of your eligible compensation, fully vested immediately) * 11 paid holidays * 15 - 25 vacation days based on years of service * Paid sick time (2.67 hours accrued bi-weekly up to a maximum of 80 hours) * In-suite exercise and relaxation room * Monthly fun events (e.g. team building activities, games, charitable events, potlucks, picnics) * Flexible and remote work schedules available for certain positions Visit our web site to learn more about us and values we embrace: <a href="https://cpcclinicalresearch.org/" target="_blank">https://cpcclinicalresearch.org/</a>. An Equal Opportunity Employer CPC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race (including traits historically associated with race, such as hair texture and length, protective hairstyles), sex, color, ancestry, sexual orientation, gender identity, gender expression, marital status, religion, creed, national origin, disability, military status, genetic information, age 40 and over or any other status protected by applicable federal, state or local law. It is our intention that all qualified applicants are given equal opportunity and that selection decisions be based on job-related factors. Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act (ADA) and certain state or local laws. If you need assistance, please email our Human Resources team at <a href="mailto:careers@cpcmed.org" target="_blank">careers@cpcmed.org</a>. 
<h3>Company Description</h3>
About CPC:\r\nCPC is an academic research organization that offers full service clinical trial design, oversight, and management with rapid access to Key Opinion Leaders in a variety of therapeutic areas. With over 35 years of experience, CPC has provided services to over 150 clinical trials in a variety of indications, with an emphasis on cardiovascular, wound healing, diabetes and more. \r\n\r\nCPC has expertise in managing clinical trials from a variety of funding sources including Industry, NIH, and Investigator Initiated trials.\r\n\r\nCPC Community Health focuses on innovative programs that reach into communities to help people find effective ways to become active, empowered and healthy. <a href="http://www.cpccommunityhealth.org/" target="_blank">http://www.cpccommunityhealth.org/</a> \r\n\r\nCPC offers:\r\n* Comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.)\r\n* Matching 401(k) plan (dollar for dollar up to 4% of your eligible compensation, fully vested immediately)\r\n* 11 paid holidays\r\n* 15 - 25 vacation days based on years of service\r\n* Paid sick time (2.67 hours accrued bi-weekly up to a maximum of 80 hours) \r\n* In-suite exercise and relaxation room\r\n* Monthly fun events (e.g. team building activities, games, charitable events, potlucks, picnics)\r\n* Flexible and remote work schedules available for certain positions\r\n\r\nVisit our web site to learn more about us and values we embrace: <a href="https://cpcclinicalresearch.org/" target="_blank">https://cpcclinicalresearch.org/</a>.\r\n\r\nAn Equal Opportunity Employer\r\nCPC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race (including traits historically associated with race, such as hair texture and length, protective hairstyles), sex, color, ancestry, sexual orientation, gender identity, gender expression, marital status, religion, creed, national origin, disability, military status, genetic information, age 40 and over or any other status protected by applicable federal, state or local law. It is our intention that all qualified applicants are given equal opportunity and that selection decisions be based on job-related factors.\r\n\r\nApplicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act (ADA) and certain state or local laws. If you need assistance, please email our Human Resources team at <a href="mailto:careers@cpcmed.org" target="_blank">careers@cpcmed.org</a>.

198 Remote Clinical Trial Manager Jobs