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Associate Clinical Research Coordinator Jobs in Reston, VA

Guidehouse

Clinical Research Coordinator

Bethesda, MD · On-site

$65K - $108K/yr

We are seeking a Clinical Research Coordinator to provide comprehensive clinical research coordination services for oncology and cancer-related clinical trials conducted within the National Cancer ...

Guidehouse

Clinical Research Coordinator

Bethesda, MD · On-site

$65K - $108K/yr

We are seeking a Clinical Research Coordinator to provide comprehensive clinical research coordination services for oncology and cancer-related clinical trials conducted within the National Cancer ...

Cape Fox SS

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Concentric Methods is seeking an experienced Clinical Research Coordinator to independently provide support services to the NIH. The total hourly pay for this non-exempt position is $30.00 for up to ...

Axle

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

Axle is seeking a Clinical Research Coordinator to join our vibrant team at the National Institutes of Health (NIH) supporting the National Cancer Institute (NCI) located in Bethesda, MD. Benefits We ...

Axle

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Axle is seeking a Clinical Research Coordinator to join our vibrant team at the National Institutes of Health (NIH) supporting the National Cancer Institute (NCI) located in Bethesda, MD. Benefits We ...

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Associate Clinical Research Coordinator information

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How much do associate clinical research coordinator jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for associate clinical research coordinator in Reston, VA is $29.84, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $32.26 per hour, depending on experience, location, and employer.

What is an associate clinical research coordinator?

Associate Clinical Research Coordinators are entry-level professionals who assist in the planning, implementation, and management of clinical trials and research studies. They support lead coordinators and principal investigators by handling tasks such as recruiting participants, collecting and entering data, ensuring regulatory compliance, and maintaining study documentation. Their role is crucial in ensuring that clinical trials run smoothly and adhere to ethical and legal standards. Associate Clinical Research Coordinators often work in hospitals, universities, or research organizations, and their work helps advance medical knowledge and patient care.

What skills and qualifications are needed to thrive as an associate clinical research coordinator?

To thrive as an Associate Clinical Research Coordinator, you need a background in life sciences or a related field, knowledge of clinical trial processes, and an understanding of regulatory requirements. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and possibly certifications like SOCRA or ACRP are typical technical assets. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating studies and interacting with diverse teams. These skills ensure studies are conducted accurately, ethically, and efficiently, supporting both compliance and successful trial outcomes.

What are the primary challenges an associate clinical research coordinator might face during a clinical trial?

One common challenge for Associate Clinical Research Coordinators is managing multiple tasks and tight timelines, as they often handle patient recruitment, data entry, and regulatory documentation simultaneously. Additionally, ensuring strict adherence to study protocols and regulatory guidelines can be complex, especially when unexpected issues arise with participants or data collection. Effective communication with the research team, principal investigators, and study participants is essential to navigate these challenges successfully and maintain the integrity of the trial.

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Associate Clinical Research Coordinator jobs near you
Infographic showing various Associate Clinical Research Coordinator job openings in Reston, VA as of August 2026, with employment types broken down into 58% Full Time, and 42% Contract. Highlights an 100% In-person job distribution, with an average salary of $62,074 per year, or $29.8 per hour.

Clinical Research Coordinator

Bethesda, MD • On-site

Cape Fox Corporation
Travel Arrangement Services • 51 - 200 employees
Learn more about Cape Fox Corporationexternal

$26 - $34.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 23 days ago

Job description

Job Title
Clinical Research Coordinator
Job Description
Concentric Methods is seeking an experienced Clinical Research Coordinator to independently provide support services to the NIH.
The total hourly pay for this non-exempt position is $30.00 for up to 40 hours per week. This rate represents the company's good faith and reasonable estimate of possible compensation at the time of posting. In addition, for eligible positions we offer a variety of benefits including specified holidays, paid leave, health insurance, dental insurance, vision insurance, life and disability insurance, tuition reimbursement, as well as 401K with company match. This job will be posted until filled or withdrawn.
Supports clinical staff develop, implement and maintain clinical research data files and materials.
- Assist preparing and submitting for review accurate source documents related to all research procedures.
Collects research data and prepares information for inputs and analysis.
- Work with staff on data acquisition and analysis using a variety of methods, including recruitment, entry, management and display for
the Department of Bioethics research studies.
Supports the development of forms and questionnaires.
- Work with staff to coordinate the logistics of courses and workshops, including the course Ethical and Regulatory Aspects of Clinical Research, and the Empirical Research Lab.
Supports the collection of data from patient charts, medical records, interviews, questionnaires, and diagnostic tests.
- Conduct literature searches; gather and synthesize background information.
Monitors subject's progress and reports adverse events.
- Assist staff writing progress reports and contributions to peer-reviewed scientific manuscripts.
Supports assembly, development and review of new research projects.
- Work with staff on manuscript preparation for research studies and manuscript submission.
- Prepare materials for IRB submission, manuscript transmittals and other necessary approvals and reviews.
Supports the creation and management of clinical websites and web-based tools.
- Collaborate with staff on the maintenance of Departmental metrics, databases and website.
Travel Requirements
0 - 10%
Job Requirements
Preferred Professional Experience:
Manuscript preparation - Data acquisition - Coordinating events - Protocol development - Statistical Analysis - Recruitment - Research
Familiarity with STATA and NVivo
Education and Certifications:
  1. Bachelor's Degree Required
  2. Two years of related experience

Core Skills:
  1. Strong organizational and time management skills.
  2. Excellent interpersonal and communication skills.
  3. Attention to detail in data collection and documentation.
  4. Proficiency in relevant computer applications and software.
  5. Ability to work both independently and collaboratively.
  6. Problem-solving and critical-thinking abilities.

Category
Science / Research
Location
Bethesda, MD - Bethesda, MD 20892 US (Primary)
Education
Bachelor's Degree

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