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Clinical Trial Associate Jobs in Reston, VA (NOW HIRING)

EDJ Associates,

Health IT Manager I

Washington, DC · On-site

$107K - $131K/yr

Employment is contingent upon EDJ Associates, Inc. receiving a contract award. This position is ... clinical trial systems, and NCI processes preferred. • Experience evaluating AI/NLP tools for ...

Guidehouse

Research Nurse

Rockville, MD · On-site

$98K - $163K/yr

Oversee clinical trial operations, participant recruitment and retention, data collection, quality ... Registered Nurse from an accredited associate's or bachelor's nursing program. * At least FOUR (4) ...

Guidehouse

Research Nurse

Rockville, MD

$98K - $163K/yr

Oversee clinical trial operations, participant recruitment and retention, data collection, quality ... Registered Nurse from an accredited associate's or bachelor's nursing program. * At least FOUR (4) ...

Amgen SA

Associate Director Study Start-up

Washington, DC · On-site

$182.15 - $212.86/hr

Requires pharma and clinical trial processes and operations expertise; no relevant therapeutic ... Associate's with 12 years OR High school diploma / GED with 14 years of clinical execution ...

New

Axle

Associate Director of AI and Data

Rockville, MD · On-site

As an Associate Director, you will combine deep technical expertise with executive presence ... and clinical trial design. This involves guiding technical teams in the application of deep ...

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All JobsClinical Trial Associate JobsClinical Trial Associate Jobs in Reston, VA

Clinical Trial Associate information

See Reston, VA salary details

$18

$41

$73

How much do clinical trial associate jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical trial associate in Reston, VA is $41.68, according to ZipRecruiter salary data. Most workers in this role earn between $33.56 and $45.87 per hour, depending on experience, location, and employer.

What is the difference between Clinical Trial Associate vs Clinical Research Coordinator?

AspectClinical Trial AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRABachelor's degree in health sciences or related field; similar certifications
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospital, academic medical centers, clinical trial sites
ResponsibilitiesAssist in trial setup, data collection, regulatory complianceManage patient recruitment, conduct visits, data entry
Industry UsageCommon in pharmaceutical and biotech industriesCommon in hospitals and academic research settings

Both roles support clinical trials but differ mainly in scope and setting. Clinical Trial Associates typically work in industry settings focusing on trial logistics and compliance, while Clinical Research Coordinators often manage patient interactions and data at clinical sites. Understanding these differences helps in choosing the right career path or job search focus.

What is a clinical trial associate?

A clinical trial associate helps oversee late-stage drug trials. They design and implement the final clinical study before making reports to the FDA and other regulatory bodies. Their duties cover logistics, including ordering supplies, auditing all reports and documents, and ensuring their timely completion. They are responsible for making sure that the trial follows all ICH and GCP requirements.

What are some common challenges faced by clinical trial associates when managing study documentation?

Clinical Trial Associates often encounter challenges related to maintaining accurate and up-to-date trial documentation, as protocols and regulatory requirements can change frequently. Ensuring all documents are correctly filed, version-controlled, and accessible for audits requires strong attention to detail and organizational skills. Additionally, coordinating with multiple stakeholders—such as clinical research coordinators, data managers, and regulatory teams—can add complexity to document management. Proactive communication and adopting robust documentation systems can help overcome these challenges.

What does a clinical trial associate do?

A Clinical Trial Associate (CTA) is responsible for supporting the planning, coordination, and management of clinical trials. They help ensure studies comply with regulatory requirements and assist in maintaining trial documentation, tracking study progress, and communicating with clinical sites. CTAs work closely with clinical research teams, sponsors, and vendors to keep trials running smoothly and efficiently. Their administrative and logistical support is essential for successful clinical research.

What are the key skills and qualifications needed to thrive as a clinical trial associate?

To thrive as a Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines, and a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, CTMS (Clinical Trial Management Systems), and GCP (Good Clinical Practice) certification are commonly required. Attention to detail, strong organizational skills, and effective communication set top performers apart in this role. These competencies are crucial for ensuring compliance, accurate data management, and smooth coordination of clinical trial activities.
More about Clinical Trial Associate jobs
What are the most commonly searched types of Clinical Trial jobs in Reston, VA? The most popular types of Clinical Trial jobs in Reston, VA are:
What are popular job titles related to Clinical Trial Associate jobs in Reston, VA? For Clinical Trial Associate jobs in Reston, VA, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Associate jobs in Reston, VA look for? The top searched job categories for Clinical Trial Associate jobs in Reston, VA are:
What cities near Reston, VA are hiring for Clinical Trial Associate jobs? Cities near Reston, VA with the most Clinical Trial Associate job openings:
Clinical Trial Associate jobs near you
Infographic showing various Clinical Trial Associate job openings in Reston, VA as of August 2026, with employment types broken down into 2% As Needed, 70% Full Time, 21% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $86,685 per year, or $41.7 per hour.

Health IT Manager I

EDJ Associates,

Washington, DC • On-site

$107K - $131K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Health IT Manager I
Department: Research
Employment Type: Full Time
Location: National Institue of Health - Washington DC Area
Description
CONTINGENT HIRE NOTICE: This position is a contingent hire. Employment is contingent upon EDJ Associates, Inc. receiving a contract award. This position is performed primarily on-site at NIH headquarters in Bethesda, Maryland. Applicants must be able to obtain and maintain a security clearance from the federal government.
The Health IT Manager I oversees task groups and provides technical authority within the CTRO and Clinical Trials Reporting Program (CTRP). This role directs analysts and programmers, leads system problem-solving with new technology, provides on-site technical direction, and coordinates across CBIIT programs to ensure effective delivery of biomedical informatics services.
Key Responsibilities
• Monitor the performance of each task or group of tasks and inform the Program Manager of all problems and accomplishments.
• Serve as the technical authority for specific task areas and participate in the resolution of systems problems with new technology.
• Direct systems analysts, programmers, and other technical personnel on assigned work.
• Coordinate across CBIIT programs and with NCI Divisions, Offices, and Centers.
• Provide on-site and remote technical direction as necessary.
• Support the identification and implementation of project management tools to meet program needs.
• Assist with the development, maintenance, and document control of project plans, roadmaps, and contract deliverable documents.
• Support data policy and process implementation for cancer research and clinical care initiatives.
• Provide consulting and technical support to government project and task managers.
• Support end-user help desk and other technical services as directed by the COR.
Skills, Knowledge and Expertise
• Minimum of three (3) years of experience in health IT management or a related discipline.
• Demonstrated ability to direct technical teams and manage complex IT projects.
• Strong problem-solving and decision-making skills.
• Knowledge of biomedical informatics, clinical trial systems, and NCI processes preferred.
• Experience evaluating AI/NLP tools for clinical data workflows preferred
• Experience with federal government contract management and reporting.
• Ability to obtain and maintain a Level 1 (Non-Sensitive) NACI background investigation.
• Project Management Professional Certification (PMP) a plus.
Tools and Technologies:
• Microsoft Office Suite (Word, Excel, PowerPoint)
• Project management and issue tracking tools
• ServiceNow or similar ticketing systems

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