Job Description
Job Description
Job Title: Clinical Research Assistant - part-time, 24 hrs/wk ONSITE
Job Description
We are seeking a dedicated Clinical Research Assistant to join our team in Salt Lake City metro, UT. This is a part-time, ONSITE position requiring 24 hours a week on a 6-month contract with potential for extension. The schedule is flexible and can be coordinated with the candidate's availability. You will perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled in clinical studies.
Responsibilities
- Verify and/or correct research study information on source documents.
- Research queries and variances and provide feedback to the site data collector.
- Input research study data into trial Electronic Data Capture systems, maintaining quality control for content, accuracy, and completeness.
- Prepare and maintain research study files.
- Compile, collate, and submit study information within established deadlines.
- Assist in the maintenance of regulatory documentation.
- Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits.
- Input visit data into Clinical Trial Management System (CTMS) to track patient visits and procedures completed against the study budget.
- Process required lab specimens, label vials, and accurately fill out requisitions for storage and/or shipment per the study protocol and packaging and shipment regulations.
- Perform various administrative support functions such as reception, office organization, and office supply management.
Essential Skills
- Basic knowledge of clinical trials.
- In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules.
- Basic knowledge of medical terminology.
- Skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word.
- Excellent interpersonal skills.
Additional Skills & Qualifications
- Knowledge of IRB communications and submissions.
- Experience in maintaining essential documents.
- Ability to recruit study subjects.
- Use of IVRS/IRT systems.
- Experience with source document preparation for remote monitoring activities.
- EMR print-out copies' certification.
- SIP maintenance.
- Patient recruitment and communication skills.
- Knowledge of protocol design for prescreening eligible patients.
- BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting such as clinical research coordinator, nurse, or medical assistant.
Work Environment
This position is office-based with a flexible part-time schedule, typically Mondays and Thursdays, with an additional day of either Tuesday or Wednesday, totaling 24 hours per week. The role involves using technologies such as EMR and clinical trial management systems and requires a tech-savvy individual. The work location is in SLC, UT metro area.
Job Type & Location
This is a Contract position based out of Salt Lake City, UT.
Pay and Benefits
The pay range for this position is $28.00 - $30.00/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 & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&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 Salt Lake City,UT.
Application Deadline
This position is anticipated to close on Jan 30, 2026.
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 actalentaccommodation@actalentservices.com for other accommodation options.