Part-Time Clinical Research Coordinator

Job Title: Clinical Research Coordinator (Part-Time, Manassas, VA)

Job Description

This part-time Clinical Research Coordinator position offers an opportunity to support an active clinical trial in Manassas, VA. Working 20 hours per week, Monday through Friday, you will focus on patient recruitment and study enrollment while ensuring adherence to protocol and regulatory standards. You will collaborate closely with participants and research staff, using your hands-on clinical research experience, strong organizational skills, and confident communication style to drive successful study outcomes.

Responsibilities

• Review medical charts thoroughly to determine eligibility against defined study criteria.
• Pre-screen potential participants using electronic medical records and study-specific requirements.
• Educate potential and enrolled participants about the clinical trial, including procedures, expectations, and protocol requirements.
• Conduct follow-up communications with participants to support retention and ensure protocol compliance.
• Schedule in-person study visits and follow-up appointments, and send reminders and relevant information to participants.
• Coordinate patient recruitment activities to meet enrollment goals for the clinical trial.
• Document interactions and study-related information accurately in the electronic medical record (EMR) and study systems.
• Collaborate with research staff to support smooth study operations in a fast-paced environment.

Essential Skills

• Proven experience working as a Clinical Research Coordinator.
• At least 2 years of patient recruitment experience in a clinical research setting.
• At least 2 years of experience working with electronic medical records (EMR).
• Formal training in HIPAA regulations and patient privacy.
• Good Clinical Practice (GCP) training and understanding of clinical research standards.
• Strong organizational skills with high attention to detail.
• Ability to communicate clearly and confidently with participants and research staff.
• Ability to manage multiple tasks and follow protocols accurately in a fast-paced environment.

Additional Skills & Qualifications

• Experience conducting chart reviews to assess eligibility for clinical trials.
• Experience in pre-screening patients for clinical studies.
• Familiarity with clinical trial recruitment strategies and participant retention practices.
• Comfort working with clinical research documentation and study workflows.
• Ability to build rapport with patients and encourage continued participation in the study.

Work Environment

This role operates during normal business hours, Monday through Friday, for approximately 20 hours per week. The environment is fast paced and detail oriented, with a strong focus on accurate chart review, effective use of electronic medical records, and timely communication with participants and research staff. You will work in a professional clinical research setting where adherence to HIPAA, GCP, and study protocols is essential.

This is a Contract position based out of Manassas, VA.

The pay range for this position is $25.00 - $33.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

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)

This is a fully onsite position in Manassas,VA.

This position is anticipated to close on Sep 9, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.