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<h3>Job Description</h3>
Job Description
Job Title: Research Assistant
Grade: 10
Salary: $42,843-$51,079
The Research Foundation for Mental Hygiene is seeking a qualified candidate to fill a full-time position of Research Assistant. Area Psychosis is seeking a full-time individual to provide research study support for an NIH-funded study focused on clinical trials. The position requires a highly organized person to manage detailed information in a research environment. The Research Assistant will assist with research study procedures, including scheduling of subjects for study procedures, conducting data entry, assisting Principal investigators in study administration, and assisting with contacting research study subjects by phone when needed. He/She will also perform some administrative duties as assigned.
Duties and Responsibilities:
<ul>
<li>Assist in organizing advertising and appointments for, and brief phone screening of potential research subjects</li>
<li>Organizing databases. </li>
<li>Help tracking and contacting patients for intake and follow up interviews in research protocols </li>
<li>Help coordinating patient appointments for psychologists and psychiatrists, and assisting psychologists and psychiatrists with research assessments </li>
<li>Help preparing data for PI to use in IRB protocol submissions and update</li>
<li>Help organizing research charts, creating some study chart documents as needed and entering data </li>
<li>Help monitoring of research charts for completeness and organizing additions and corrections as needed </li>
<li>Assist in the communication with the study supervisor, inpatient unit, and pharmacy as needed </li>
<li>If applicable, assist in training new hires to assume incumbent responsibilities</li>
</ul>
Minimum Qualifications:
<ul>
<li>Bachelor's degree in health, psychology medical science or related field.</li>
</ul>
Preferred Qualifications:
<ul>
<li>At least (1) year of clinical experience conducting diagnostic and clinical interviews preferred.</li>
</ul>
 
Work Location: 1051 Riverside Drive, New York, NY-10032
To Apply: Submit an application through our website at <a href="https://rfmh.applicantpro.com/jobs/" target="_blank">https://rfmh.applicantpro.com/jobs/</a>. Please note only applications submitted through our website will be considered.
The Mission of the Research Foundation for Mental Hygiene, Inc. (RFMH) is to promote the mental health of all New Yorkers, with a focus on providing hope and supporting recovery for adults with serious mental illness and children with serious emotional disturbances. Applicants with lived mental health experience are encouraged to apply. RFMH is deeply committed to supporting underserved individuals, organizations, and communities. To this end, RFMH is focused on implementing activities and initiatives to reduce disparities in access, quality, and treatment outcomes for underserved populations. A critical component of these efforts is ensuring that RFMH is a diverse and inclusive workplace where all employees' unique attributes and skills are valued and utilized to support the mission of the Agency. RFMH is an equal opportunity/affirmative action employer.
The Research Foundation is a private not-for-profit corporation and is not an agency or instrumentality of the State of New York. Employees of the Research Foundation are not state employees, do not participate in any state retirement system, and do not receive state fringe benefits. Excellent Benefits Package. Affirmative Action/Equal Opportunity Employer - Disabled/Veteran, 41 CFR 60-741.5(a) and 41 CFR 60-300.5(a) compliant.
 
 Job Posted by ApplicantPro

Research Assistant

<h3>Job Description</h3>
Job DescriptionJob Title: QC Microbiology Compliance Investigator
Job Description
As a QC Microbiology Compliance Investigator, you will play a pivotal role in determining the causes and preventative actions of Deviations, Non-Conformances, Out of Specifications (OOS), Out of Trends (OOT), and environmental excursion investigations. You will drive investigations to their true root cause using appropriate tools, benchmark industry standards, and implement investigative and impact assessment toolsets. Your work will define and implement effective preventative actions to prevent recurrence while managing multiple investigations efficiently.
Responsibilities
<ul>
<li>Collaborate with cross-functional teams to develop and track CAPA plans.</li>
<li>Identify and create appropriate trending rules that trigger corrective actions.</li>
<li>Analyze process data and evaluate trends to identify major improvement opportunities.</li>
<li>Effectively utilize change management approaches.</li>
<li>Develop materials to train personnel on writing problem statements and using root cause analysis tools.</li>
<li>Manage CAPA plans and their implementation.</li>
<li>Communicate plans for ongoing deviations and CAPAs effectively.</li>
<li>Oversee the timely completion of deviations, CAPAs, and Change Controls.</li>
<li>Abide by quality standards and ensure compliance.</li>
</ul>
Essential Skills
<ul>
<li>Expertise in laboratory processes, CAPA, Bioburden, and Aseptic techniques.</li>
<li>Experience in investigations and analysis, including life-cycle investigations of deviations and non-conformances.</li>
<li>GMP Training, Quality Systems Training, and Safety Training.</li>
<li>Experience with QC Micro deviations and compliance in microbiology.</li>
<li>Knowledge of U.S. and international cGMPs, ICH, and other regulations.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor of Science in a Quality/Process-related field or equivalent experience.</li>
<li>3-5 years of experience in quality control or assurance within the bio-pharma, biologics, or pharmaceutical industry.</li>
<li>Experience leading event investigations, Root Cause Analysis (RCA), and CAPA.</li>
<li>Technical experience in writing and assessing deviations, investigations, and OOS.</li>
<li>Strong IT skills, including proficiency with Visio, Microsoft Project, and Excel.</li>
<li>Experience using e-Quality Management Systems is preferred.</li>
</ul>
Work Environment
You will work in a GMP Commercial Facility with a schedule of Monday to Friday on the 1st shift. Flexibility is essential. The work environment offers a great atmosphere, opportunities for growth, and the chance to be part of a new project taking a client's product commercial.
Pay and Benefits
The pay range for this position is $45.55 - $45.55/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Allendale,NJ.
Application Deadline
This position is anticipated to close on Oct 24, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

QC Microbiology Compliance Investigator

<h3>Job Description</h3>
Job DescriptionRadical AI, Inc.&nbsp;is an artificial intelligence company that is accelerating scientific research &amp; development. We are at the forefront of innovation in the field of materials R&amp;D, a critical driver for advancing our most cutting-edge industries and shaping the future. Breaking away from the traditionally slow and costly R&amp;D process, Radical AI leverages artificial intelligence and machine learning to pioneer generative materials science. This innovative field blends AI, engineering, and materials science, revolutionizing how materials are created and discovered. Radical AI's approach speeds up R&amp;D and addresses global challenges, setting new benchmarks in technology and sustainability. The OpportunityAs a Computational Materials Scientist, you will be engaging in critical simulations and modeling for materials discovery, development, and characterization. Your expertise with ab-initio calculations, DFT, and other forms of computational and theory-based modeling will be crucial to our AI-driven discovery process. You will work with leading AI scientists who depend on you to assist in data aggregation, data generation, materials simulation and model development. You will draw on a robust background in computational chemistry, software development, and machine learning. You will be responsible for running AI-enabled computational workflows for materials discovery, serving as a critical resource to the ML and materials research teams.About you
<ul>
<li>PhD degree in Chemistry, Materials Science, Computational Chemistry, Chemical Engineering, or another related subject.</li>
<li>Strong research experience (e.g., evidenced by publication record), including experience in computational modeling, utilizing ab-initio methods, and coarse-graining potentials for multiscale simulations of atomistic systems.</li>
<li>Understanding of the fundamental mechanics of metals and how to model them computationally.</li>
<li>Experience running high-throughput DFT.</li>
<li>Experience with interatomic potentials.</li>
<li>Chemistry software development experience (preferably public on e.g. GitHub, please share links to high impact pull request).</li>
<li>Experience coding in Python or other similar languages.</li>
</ul>
Pluses
<ul>
<li>Running high-throughput DFT workflows at the order of 5,000+ concurrent jobs.</li>
<li>Prior experience in transitioning AI + computational research into production environments.</li>
<li>Experience with additional ICME approaches (e.g., mechanistic structure-property modeling, Phase Field, CALPHAD, Atomistics, Molecular statics/dynamics, etc.).</li>
<li>Experience with FEM software tools (e.g., ANSYS, ABAQUS, MOOSE, PRISMS).</li>
<li>Experience with metal additive manufacturing techniques.</li>
</ul>
Salary Description Competitive salary + Equity + Benefits; base pay offered may vary depending on job-related knowledge, skills, and experience. Disclosure Radical AI is committed to equal employment opportunity regardless of race, color, ancestry, national origin, religion, sex, age, sexual orientation, gender identity and expression, marital status, disability, or veteran status.

Computational Chemist/Material Scientist - Metal Alloys

<h3>Job Description</h3>
Job DescriptionJob Title: QC Microbiology Compliance Investigator
Job Description
As a QC Microbiology Compliance Investigator, you will play a pivotal role in determining the causes and preventative actions of Deviations, Non-Conformances, Out of Specifications (OOS), Out of Trends (OOT), and environmental excursion investigations. You will drive investigations to their true root cause using appropriate tools, benchmark industry standards, and implement investigative and impact assessment toolsets. Your work will define and implement effective preventative actions to prevent recurrence while managing multiple investigations efficiently.
Responsibilities
<ul>
<li>Collaborate with cross-functional teams to develop and track CAPA plans.</li>
<li>Identify and create appropriate trending rules that trigger corrective actions.</li>
<li>Analyze process data and evaluate trends to identify major improvement opportunities.</li>
<li>Effectively utilize change management approaches.</li>
<li>Develop materials to train personnel on writing problem statements and using root cause analysis tools.</li>
<li>Manage CAPA plans and their implementation.</li>
<li>Communicate plans for ongoing deviations and CAPAs effectively.</li>
<li>Oversee the timely completion of deviations, CAPAs, and Change Controls.</li>
<li>Abide by quality standards and ensure compliance.</li>
</ul>
Essential Skills
<ul>
<li>Expertise in laboratory processes, CAPA, Bioburden, and Aseptic techniques.</li>
<li>Experience in investigations and analysis, including life-cycle investigations of deviations and non-conformances.</li>
<li>GMP Training, Quality Systems Training, and Safety Training.</li>
<li>Experience with QC Micro deviations and compliance in microbiology.</li>
<li>Knowledge of U.S. and international cGMPs, ICH, and other regulations.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor of Science in a Quality/Process-related field or equivalent experience.</li>
<li>3-5 years of experience in quality control or assurance within the bio-pharma, biologics, or pharmaceutical industry.</li>
<li>Experience leading event investigations, Root Cause Analysis (RCA), and CAPA.</li>
<li>Technical experience in writing and assessing deviations, investigations, and OOS.</li>
<li>Strong IT skills, including proficiency with Visio, Microsoft Project, and Excel.</li>
<li>Experience using e-Quality Management Systems is preferred.</li>
</ul>
Work Environment
You will work in a GMP Commercial Facility with a schedule of Monday to Friday on the 1st shift. Flexibility is essential. The work environment offers a great atmosphere, opportunities for growth, and the chance to be part of a new project taking a client's product commercial.
Job Type &amp; Location
This is a Contract to Hire position based out of Allendale, New Jersey.
Pay and Benefits
The pay range for this position is $45.55 - $45.55/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Allendale,NJ.
Application Deadline
This position is anticipated to close on Nov 3, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
In this role, you will apply Biophysical analytical skills in biotherapeutic drug products characterization with focus on product robustness. You will be working in a collaboratively team environment to support both early and late stage formulation development
<ul>
<li>Execute&nbsp;assays such as MFI, SEC-MALS, Intrinsic Fluorescence, Infrared Spectroscopy, UV Circular Dichroism, DLS, and DSC to support the particle characterization and stability analysis</li>
<li>Created and maintained record of all experiment execution in Electronic Laboratory Notebook (ELN) adhering to Good Laboratory Practice and Good documentation practice (GDP)</li>
<li>Perform Safety Standard Testing of lab instruments and troubleshooting instrument errors</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>BS/MS in Biophysics, Biochemistry, Chemistry, Chemical Engineer, Biomedical Engineering, Pharmaceutical Sciences or related discipline</li>
<li>1 to 2 years of expertise in operating various Biophysical instruments including but not limited to HIAC,&nbsp;SEC-MALS, MFI, FTIR; good understanding of protein science, protein/peptide stability, and protein-protein interactions</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
This position is Full-Time,&nbsp;Monday - Friday, 8:00&nbsp;a.m. - 5:00&nbsp;p.m. Candidates currently living within a commutable distance of&nbsp;Rahway, NJ&nbsp;are encouraged to apply.&nbsp;Compensation range is between $24-25.50/hr considering experience.
<ul>
<li>Excellent full time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Biophysical Analytical Scientist

<h3>Job Description</h3>
Job Description
Description HistoWiz is the largest online histopathology company, based in New York City. Our mission is to help biomedical researchers find cures by accelerating histopathology and enabling global collaboration.
Since inception in 2013, we have doubled our month-over-month sales, driven primarily by customer referrals. We are profitable, won numerous awards and are funded by prestigious investors, including Y-Combinator and Zhenfund. We are seasoned scientists with experience at leading academic institutions and have published high impact research in top journals of biomedicine. We have just completed our Series A and are now looking to scale our business significantly in the coming years.
HistoWiz has over 3,000 paying customers globally from top academic institutions (e.g. MSKCC, Harvard, Stanford, HHMI) and pharmaceutical companies (e.g. CRISPR, Johnson &amp; Johnson, Regeneron). We process tissue specimens and digitize all of the results, hosting our client’s data on a proprietary platform, PathologyMapTM . This platform not only enables industry-leading turnaround time for diagnosis, but also online viewing, sharing and search. No other platform like this exists, so we are truly building something new that can bridge scientists, doctors, and patients from all over the world to conquer life-threatening diseases collaboratively instead of individually. This online platform also contains the world’s largest collection of pathology data and the first network of top pathologists.
We are looking for highly motivated Research Associate to join our fast-growing team. Under the general direction and supervision of the Director of Laboratory Operations, the Research Associate will effectively apply a working knowledge and skill of designated Research Associate-related duties and tasks, in support of the Department as a whole, to complete the daily assigned Histology workload. &nbsp;
Requirements
<ul>
<li>Research and review the literature to find the best antibodies for IHC and IF</li>
<li>Design and recommend processes, systems, and operational changes to increase efficiency and effectiveness</li>
<li>Maintain laboratory organization and team priorities to complete projects with client-expected turnaround time</li>
<li>Lead project update meetings with clients</li>
<li>Design experiments and interpret results, while thinking critically about research projects</li>
<li>Write IHC validation reports for pharma clients</li>
<li>Coordinate in ordering supplies and maintain inventory for the AIR department</li>
<li>Develop new protocols and assays, including Multiplex mIF panels</li>
<li>Troubleshoot quality issues and work with pathologists to QC slides</li>
<li>Oversee and perform biomarker and equipment validations</li>
<li>Perform IHC, IF and ISH via RNAScope independently</li>
</ul>
Position Requirements:
<ul>
<li>Bachelors degree in scientific field preferred</li>
<li>Tech-savvy, fast learner. We use a proprietary, digital LIMS system</li>
<li>Strong verbal and written communication skills</li>
<li>HTL or QIHC licenses, a plus</li>
<li>Experience working at a biotech&nbsp;preferred</li>
</ul>
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m1E3ZQAURt

Research Associate

<h3>Job Description</h3>
Job DescriptionOverview Ansible Government Solutions, LLC (Ansible) is currently recruiting a Therapeutic Medical Physicist to provide onsite services to eligible beneficiaries of the East Orange VA New Jersey Healthcare System located at 385 Tremont Avenue, East Orange, NJ 07018.&nbsp; If you accept employment with Ansible, you must also acknowledge that any assigned schedule is subject to change at the direction of either Ansible or its customers. Ansible Government Solutions, LLC (Ansible) is a Service-Disabled Veteran-Owned Small Business (SDVOSB) providing Federal customers with solutions in many arenas. Our customers face wide-ranging challenges in the fields of national security, health care, and information technology. To address these challenges, we employ intelligent and committed staff who take care of our customers’ success as if it is their own. Responsibilities&nbsp;
<ul>
<li>Radiation treatment planning and dose delivery optimization.</li>
<li>Radiation protection for patients and staff.</li>
<li>Presence during complex procedures (SRS, SBRT, IGRT).</li>
<li>Weekly and final chart reviews for all radiation therapy patients.</li>
<li>Dosimetry and QA for treatment planning systems and equipment.</li>
<li>Peer review participation and documentation.</li>
<li>Support for direct patient care (90–95% involvement for radiation therapy technologists).</li>
<li>Calibration and testing of radiation therapy equipment.</li>
<li>Maintenance and QA of treatment planning software and hardware.</li>
<li>Documentation of QA activities and performance metrics.</li>
<li>Support for acquisition and evaluation of radiation-producing machines.</li>
<li>Network and computer support for radiotherapy systems.</li>
<li>Participation in quality improvement meetings and staff meetings.</li>
<li>Compliance with VA patient safety and incident reporting protocols.</li>
<li>Documentation in VA’s CPRS system with proper coding and electronic signatures.</li>
<li>Attendance tracking and invoice verification.</li>
</ul>
Qualifications
<ul>
<li>Master's degree in Medical Physics or related field&nbsp;</li>
<li>Board Certification in Medical Physics or Therapeutic Medical Physics by the American Board of Radiology (ABR)&nbsp;</li>
<li>Minimum 2 years of continuous working experience within the last 3 years in therapeutic medical physics&nbsp;</li>
<li>Experience with:&nbsp;
<ul>
<li>Varian Linear Accelerators (TrueBeam with Brain Lab Accessories)&nbsp;</li>
<li>Image Guided Radiation Therapy (IGRT) including Cone Beam CT&nbsp;</li>
<li>Eclipse treatment planning system and ARIA record &amp; verify system&nbsp;</li>
<li>Treatment modalities including 2D/3D Conformal, SRS, SRT, SBRT, and IMRT/VMAT&nbsp;</li>
<li>IMRT QA systems (e.g.,&nbsp;MapCheck)&nbsp;</li>
<li>CT Simulators&nbsp;</li>
<li>Superficial X-ray machines&nbsp;</li>
</ul>
</li>
<li>Experience in a healthcare system with ACR or&nbsp;APEx&nbsp;certification preferred&nbsp;</li>
<li>Strong analytical and problem-solving skills&nbsp;</li>
<li>Excellent communication and teamwork abilities&nbsp;</li>
<li>Proficiency&nbsp;in computer systems and networking related to radiation oncology&nbsp;</li>
<li>Ability to pass a government background check and complete required VA training&nbsp;</li>
</ul>
All candidates must be able to:
<ul>
<li>Sit, stand, walk, lift, squat, bend, twist, and reach above shoulders during the work shift</li>
<li>Lift up to 50 lbs from floor to waist</li>
<li>Lift up to 20 lbs</li>
<li>Carry up to 40 lbs a reasonable distance</li>
<li>Push/pull with 30 lbs of force</li>
</ul>
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. 
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6FuC94Pd8m

Therapeutic Medical Physicist

<h3>Job Description</h3>
Job Description
About Us ISMG is a global media powerhouse and intelligence firm at the forefront of cybersecurity, enterprise IT, and digital transformation. With 10+ trusted media brands, 38+ digital properties, and 400+ executive events annually, ISMG reaches a network of 2M+ business leaders, CISOs, regulators, and technology innovators worldwide. We are entering an extraordinary growth phase—expanding our editorial depth and global reach. If you’re passionate about shaping narratives that influence the world of cybersecurity and financial services, this is your moment to lead. The Opportunity We are hiring an experienced journalist to serve as Senior Correspondent and lead content creator for ISMG's flagship media property,&nbsp;BankInfoSecurity. This senior editorial role focuses on delivering high-impact, multimedia journalism for a global audience of banking, fintech, and cybersecurity professionals. You will drive content strategy, manage the editorial calendar, and produce compelling storytelling across formats—including in-depth articles, blogs, video/audio interviews, webinars, and live events. Collaborating with subject matter experts worldwide, you’ll lead coverage on key industry trends such as cyber fraud, regulatory changes, digital identity, AI in banking, and ransomware. This position is ideal for a self-starter who thrives in a dynamic environment and excels as part of an international, award-winning editorial team. Key Responsibilities
<ul>
<li>Lead the creation and curation of timely, engaging, and authoritative content for BankInfoSecurity and CUInfoSecurity.</li>
<li>Produce and edit news articles, thought leadership blogs, investigative features, and original video/audio interviews.</li>
<li>Develop and maintain an editorial calendar in alignment with industry events, regulatory updates, and breaking news.</li>
<li>Ensure all content meets ISMG’s editorial standards, SEO best practices, and audience engagement benchmarks.</li>
<li>Conduct interviews with senior banking, cybersecurity, and compliance executives.</li>
<li>Curate expert speaker panels and moderate sessions for ISMG's global summits and CISO roundtables, producing event coverage and securing interviews.</li>
<li>Researching and staying up-to-date with current industry and technology trends, as well as security regulations/guidance and relevant legislative activities.</li>
<li>Providing editorial support to other sectors covered by ISMG.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree in Journalism, Communications, or related field—or equivalent experience.</li>
<li>10+ years of professional B2B journalism experience, preferably covering banking, fintech, cybersecurity, or information technology.</li>
<li>5+ years focused on banking security or financial regulatory reporting.</li>
<li>Strong knowledge of cyber threat trends, digital fraud, regulatory compliance, and risk management in financial services.</li>
<li>Knowledge of regulatory bodies and the guidance issued by these bodies for providing a framework for information security within all sectors.</li>
<li>Track record of breaking news, industry scoops, and thought leadership reporting.</li>
<li>Excellent communication, editorial judgment, and ability to work autonomously in a global remote environment, collaborating with a variety of internal and external personas.</li>
<li>Experience managing or mentoring junior editors or freelance contributors is a plus.</li>
<li>Relationships with financial CISOs, compliance officers, regulators, and tech leaders is a plus.</li>
</ul>
🎯Why Join ISMG?
<ul>
<li>Be part of a globally recognized editorial team with unmatched access to C-level decision-makers.</li>
<li>Shape critical narratives in cybersecurity and finance at a pivotal time.</li>
<li>Work with purpose in a mission-driven, innovative media environment.</li>
</ul>
👉&nbsp;Ready to part of something bigger?&nbsp;Apply now or visit&nbsp;ISMG.io&nbsp;to learn more!
<ul>
<li>📍Location: Manhattan, NY (on-site Monday–Friday)</li>
<li>&amp;#x1F4B0;Salary Range: $120,000 to $140,000 (negotiable dependent on experience level)</li>
</ul>
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L8qYgxBaR3

Senior Correspondent, BankInfoSecurity

<h3>Job Description</h3>
Job Description
About Us ISMG&nbsp;is a global media powerhouse and intelligence firm at the forefront of cybersecurity, enterprise IT, and digital transformation. With 10+ trusted media brands, 38+ digital properties, and 400+ executive events annually, ISMG reaches a network of 2M+ business leaders, CISOs, regulators, and technology innovators worldwide. We are entering an extraordinary growth phase—expanding our editorial depth and global reach. If you’re passionate about shaping narratives that influence the world of cybersecurity and business technology, this is your moment to lead. The Opportunity CIO.inc, ISMG’s media platform for CIOs and technology leaders, is seeking a&nbsp;Senior Correspondent &amp; Managing Editor&nbsp;to lead high-impact editorial coverage across North America and adjoining geographies. Partnering with our India-based editorial team, you’ll bring a global lens to enterprise IT, cybersecurity, and digital transformation—while shaping editorial strategy, driving original reporting, and engaging directly with senior technology executives in the U.S. market. This senior-level role is ideal for a journalist who thrives at the intersection of technology and business leadership. You’ll gain visibility within a worldwide CIO and CISO community, influence industry thought leadership, and have opportunities to moderate global events while collaborating with some of the most innovative minds in tech. Key Responsibilities
<ul>
<li>Report and write an engaging mix of news articles, features, analysis/opinion pieces and executive interviews (text, audio and video).</li>
<li>Build relationships with CIOs, CTOs and industry leaders to produce engaging and exclusive stories.</li>
<li>Host conversations and panel discussions with senior IT leaders through webinars, LinkedIn panels and at key ISMG summits and events.</li>
<li>Work closely with the global editorial, social media and events teams to grow CIO.inc’s reach and influence.</li>
<li>Stay up-to-date on enterprise tech, cybersecurity and regulatory trends to bring clarity and authority to our coverage.</li>
</ul>
Requirements
<ul>
<li>6–10 years in journalism, ideally covering the CIO community, enterprise technology, cybersecurity and business IT.</li>
<li>Ability to generate suitable story ideas, conduct insightful executive interviews and deliver clear, compelling reporting.</li>
<li>Comfortable moderating panels, hosting interviews and presenting at events.</li>
<li>Experience in building and engaging professional audiences through reporting, events or digital platforms.</li>
<li>Strong grasp of enterprise IT, digital business transformation, security and emerging technologies.</li>
</ul>
Why Join Us?
<ul>
<li>Be part of a globally recognized editorial team with unmatched access to C-level decision-makers.</li>
<li>Shape critical narratives in cybersecurity and business&nbsp;technology at a pivotal moment.</li>
<li>Work with purpose in a mission-driven, innovative environment.</li>
</ul>
👉&nbsp;Ready to part of something bigger? Apply now or visit&nbsp;ISMG.io&nbsp;to learn more!
<ul>
<li>📍Location: Manhattan, NY (on-site, Monday–Friday)</li>
<li>&amp;#x1F4B0;Salary Range: $120,000 to $140,000 (dependent on experience level)</li>
</ul>
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Senior Correspondent, CIO.inc

<h3>Job Description</h3>
Job Description
IIRR is one of the world’s leading rural development NGOs. Founded in 1960, IIRR’s programs have impacted more than 62 million rural lives across five continents. The organization’s programs address the health, education, and environmental conditions of rural communities and prioritizes the delivery of sustainable and scalable solutions that empower people to improve their lives and livelihoods. IIRR maintains offices in Africa, Asia, and North America.&nbsp;&nbsp;&nbsp;&nbsp;
IIRR is looking for intelligent, strategic, and resourceful thinkers to help support the development of project proposals and knowledge management materials through targeted research activities. Research Officer Interns will work under the direction of the Director of Global Operations.&nbsp;&nbsp;
This is an unpaid internship but available for class credits. We have two internship models:&nbsp;&nbsp;
(i) full-time - requires a 5 days (40 hours) a week commitment of 3 months&nbsp;&nbsp;&nbsp;
(ii) part-time - required 3 to 4 days (20 hours) a week commitment of 6 months.&nbsp;
Please note that internship hours must be scheduled during regular New York/East Coast business hours.&nbsp;
Responsibilities may include one or more of the following:&nbsp;&nbsp;
<ul>
<li>Review literature relevant to IIRR’s flagship themes: Health, Education, Economic Empowerment, Food Systems, and the Environment&nbsp;</li>
<li>Contribute input to the development of research questions &amp; concept notes&nbsp;</li>
<li>Assist in authoring research reports, briefing notes, policy papers, and other materials as required&nbsp;</li>
<li>Research and Identify and develop possible areas for partnership with local organizations, universities, research institutions, etc.&nbsp;&nbsp;</li>
<li>Represent IIRR where appropriate in program meetings, coordination meetings, staff meetings, workshops, and meetings with stakeholders&nbsp;</li>
<li>Help to develop and coordinate research dissemination and follow-up activities, including providing substantive advice on the future direction of the program&nbsp;</li>
<li>Other duties as required&nbsp;</li>
</ul>
&nbsp;Requirements:&nbsp;
<ul>
<li>Bachelor’s degree in any discipline (completed prior to internship start date)</li>
<li>Well-organized, reliable, and self-motivated&nbsp;&nbsp;</li>
<li>Helpful and responsive (e.g., when dealing with ad-hoc requests for providing support)</li>
<li>Resourceful, creative, who enjoys problem-solving&nbsp;</li>
<li>Impeccable writing skills with meticulous attention to detail and organizational skills&nbsp;</li>
<li>Curiosity, creativity, and fearlessness in contributing new and bold ideas&nbsp;</li>
<li>Exceptional interpersonal skills&nbsp;</li>
<li>Ability to meet deadlines and effectively multi-task&nbsp;</li>
<li>A willingness to fail fast and forward while respecting and valuing input from a global and diverse team&nbsp;</li>
<li>Ability and willingness to work in a startup culture that may require fluidity in roles from week to week&nbsp;&nbsp;</li>
<li>Intermediate experience with MS Word, Excel, PowerPoint, Google Applications&nbsp;</li>
<li>Responsive to manager’s feedback, ability to take direction and execute work independently with minimal oversight in a remote working environment</li>
<li>Passionate about making a positive difference</li>
</ul>
Application Instructions:
Submit resume/CV, cover letter (indicating preference for part-time or full-time placement), and contact information for three references.
Applications will be reviewed on a rolling basis until the position is filled.&nbsp;
No calls, please. If you have not received a response from us in two weeks, you should assume that your application was not successful on this occasion.&nbsp;
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676 Science Jobs in New York, NY 10007, USA