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Clinical Research Project Assistant Jobs in Reston, VA

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 ... Monitor project performance and identify potential barriers to success * Assist investigators and ...

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 ... Monitor project performance and identify potential barriers to success * Assist investigators and ...

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 ... Monitor project performance and identify potential barriers to success * Assist investigators and ...

Monitor study timelines and assist with tracking project deliverables. * Communicate effectively ... Ensure research activities are conducted in compliance with ICH Good Clinical Practice (GCP), study ...

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

Monitors subject's progress and reports adverse events. - Assist staff writing progress reports and ... Supports assembly, development and review of new research projects. - Work with staff on manuscript ...

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Monitors subject's progress and reports adverse events. - Assist staff writing progress reports and ... Supports assembly, development and review of new research projects. - Work with staff on manuscript ...

Research Assistant

Bethesda, MD · On-site +1

$57K - $60K/yr

This position will support project teams in completion of commercial and government clinical ... clinical research methodologies to meet protocol and regulatory requirements. • Assist in the ...

This position will support project teams in completion of commercial and government clinical ... Apply basic clinical research methodologies to meet protocol and regulatory requirements. Assist in ...

Research Assistant

Bethesda, MD · Remote

$57K - $60K/yr

This position will support project teams in completion of commercial and government clinical ... clinical research methodologies to meet protocol and regulatory requirements. • Assist in the ...

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Dependent Care Assistant Program (DCAP) * Transportation Reimbursement Account (TRN) Position ... Strong organizational, communication, and project coordination skills * Demonstrated experience ...

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

Dependent Care Assistant Program (DCAP) * Transportation Reimbursement Account (TRN) Position ... Strong organizational, communication, and project coordination skills * Demonstrated experience ...

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Dependent Care Assistant Program (DCAP) * Transportation Reimbursement Account (TRN) Position ... Strong organizational, communication, and project coordination skills * Demonstrated experience ...

Coordinate multiple clinical research studies simultaneously. * Assist with onboarding activities ... Strong organizational and project coordination skills * Effective communication skills The annual ...

Coordinate multiple clinical research studies simultaneously. * Assist with onboarding activities ... Strong organizational and project coordination skills * Effective communication skills The annual ...

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Clinical Research Project Assistant information

See Reston, VA salary details

$8

$23

$48

How much do clinical research project assistant jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for clinical research project assistant in Reston, VA is $23.63, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $27.02 per hour, depending on experience, location, and employer.

What do clinical research assistants do?

Clinical research assistants support the conduct of clinical trials by preparing study materials, recruiting and screening participants, collecting and managing data, and ensuring compliance with protocols and regulations. They often work under the supervision of investigators and may use electronic data capture tools or databases as part of their responsibilities.

What is the difference between Clinical Research Project Assistant vs Clinical Research Coordinator?

AspectClinical Research Project AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCR are common
Work EnvironmentSupports research teams in clinical settings, hospitals, or research institutionsManages daily clinical trial activities, interacts directly with patients and investigators
Employer & Industry UsageUsed by research institutions, hospitals, pharmaceutical companiesCommonly employed in clinical trial sites, hospitals, and research organizations

The Clinical Research Project Assistant primarily supports research activities and data management, while the Clinical Research Coordinator oversees trial operations and patient interactions. Both roles require similar educational backgrounds and certifications, but their responsibilities differ in scope and daily tasks.

How much money do clinical research assistants make?

Clinical research assistants typically earn a median annual salary of around $45,000 to $55,000, depending on experience, location, and the complexity of the research environment. Entry-level positions may start lower, while those with specialized skills or certifications can earn higher wages.

What does a research project assistant do?

A research project assistant supports the planning, coordination, and execution of clinical research studies. They handle tasks such as data collection, maintaining study documentation, scheduling participant visits, and ensuring compliance with protocols and regulations. Strong organizational skills and familiarity with research tools like electronic data capture systems are often required.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, such as a background in healthcare or life sciences, and often involves monitoring clinical trials. Entry-level roles in clinical research may include Clinical Trial Assistant or Research Coordinator, with CRAs generally needing several years of related experience or specialized training. Certifications like SOCRA or ACRP can also be beneficial for advancing to CRA roles.
What are the most commonly searched types of Clinical Research Project jobs in Reston, VA? The most popular types of Clinical Research Project jobs in Reston, VA are:
What are popular job titles related to Clinical Research Project Assistant jobs in Reston, VA? For Clinical Research Project Assistant jobs in Reston, VA, the most frequently searched job titles are:
What job categories do people searching Clinical Research Project Assistant jobs in Reston, VA look for? The top searched job categories for Clinical Research Project Assistant jobs in Reston, VA are:
What cities near Reston, VA are hiring for Clinical Research Project Assistant jobs? Cities near Reston, VA with the most Clinical Research Project Assistant job openings:
Infographic showing various Clinical Research Project Assistant job openings in Reston, VA as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 1% Temporary, and 3% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $49,147 per year, or $23.6 per hour.
Clinical Research Coordinator

Clinical Research Coordinator

Axle

Bethesda, MD • On-site

$26 - $34.50/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago


Job description

(ID: 2026-2878)
Axle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH).
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 Offer:
  • 100% Medical, Dental & Vision Coverage for Employees
  • Paid Time Off and Paid Holidays
  • 401K match up to 5%
  • Educational Benefits for Career Growth
  • Employee Referral Bonus
  • Flexible Spending Accounts:
    • Healthcare (FSA)
    • Parking Reimbursement Account (PRK)
    • Dependent Care Assistant Program (DCAP)
    • Transportation Reimbursement Account (TRN)

Position Overview
The Contractor shall provide personnel capable of supporting complex clinical research portfolios and ensuring efficient coordination among investigators, research teams, oversight offices, regulatory agencies, collaborating institutions, and other stakeholders involved in the conduct of clinical research. Requires a Master's degree, along with preferred certifications such as SOCRA, FAC-P/M, FAC-COR, PMP, or ACRP credentials. Experience with clinical trial management systems and research databases, technology transfer or clinical trial agreements, and supporting NIH, NCI, academic medical centers, or federally funded research programs is preferred.
Additional Qualifications
Certifications & Licenses
  • SOCRA Certification
  • FAC-P/M Certification
  • FAC-COR Certification
  • PMP Certification
  • Association of Clinical Research Professionals (ACRP)

Field of Study
  • Health and Medical Administrative Services
  • Nursing

Software
  • Experience with clinical trial management systems and research database

Skills
  • Experience with technology transfer agreements, clinical trial agreements, cooperative research and development agreements, or related research partnerships
  • Experience supporting NIH, NCI, academic medical centers, or federally funded research programs

Deliverables
  • Monthly Activity Report - Monthly
  • Portfolio Status Report - Monthly
  • Risk Management Report - Monthly
  • Financial Status Report - Monthly
  • Regulatory Tracking Report - Monthly
  • Strategic Planning Support Reports - Ad-Hoc
  • Annual Program Summary Report - Yearly
  • Final Contract Summary Report - Ad-Hoc

Statement of Work Details
  • Coordinate operational activities for clinical studies - 1
  • Assist with feasibility assessments for proposed clinical trials - 2
  • Support startup activities for new studies - 3
  • Coordinate participating sites for multi-center trials - 4
  • Monitor study progress and enrollment-related metrics - 5
  • Reviews, assesses and evaluates clinical trial design and feasibility
  • Provide comprehensive management and oversight of assigned clinical research portfolios
  • Develop and maintain project management plans for clinical research projects
  • Monitor project schedules, timelines, deliverables, dependencies, and milestones
  • Track portfolio performance metrics and report progress to leadership
  • Assist Branch Chiefs and Program Leadership in prioritization of research activities
  • Support portfolio planning and resource allocation efforts
  • Monitor project execution to ensure alignment with organizational objectives
  • Reviews, evaluates and analyzes clinical trial data and study information
  • Lead development and maintenance of project-specific work plans
  • Coordinate project initiation, planning, execution, monitoring, and closeout activities
  • Facilitate project meetings and maintain meeting documentation
  • Track action items and follow-up activities
  • Monitor project performance and identify potential barriers to success
  • Assist investigators and research teams in achieving project objectives
  • Reviews, evaluates and recommends logistical, procedural and operational approaches to clinical trial implementation
  • Develop risk mitigation and response plans
  • Monitor identified risks throughout the project lifecycle
  • Escalate significant issues to leadership as appropriate
  • Coordinate corrective actions and resolution activities
  • Identify operational, regulatory, financial, and programmatic risks
  • Assesses and supports meetings, clinical trial assessments and site visits
  • Monitor and coordinate activities associated with protocol development, protocol amendments, IRB submissions, regulatory submissions, continuing reviews, study activation activities, and clinical trial monitoring activities
  • Support preparation for audits, inspections, and monitoring visits
  • Coordinate activities among investigators, regulatory staff, data managers, and clinical teams
  • Monitor compliance-related milestones and deliverables
  • Facilitate timely submission of required regulatory documents
  • Formulates guiding principles and Standard Operating Procedures (SOPs), and prepares staff for clinical research
  • Facilitate communication among study stakeholders
  • Assist with development of project-specific budgets
  • Monitor expenditures and financial performance
  • Track project funding and resource utilization
  • Develop financial forecasts
  • Identify potential budgetary concerns and recommend corrective actions
  • Prepare financial status reports for leadership review
  • Serve as liaison between assigned research programs and the Office of the Clinical Director (OCD), NCI Technology Transfer Center, regulatory offices, collaborating institutions, industry partners, and other NIH and NCI organizations
  • Coordinate leadership briefings and status updates
  • Prepare communication materials and project summaries
  • Assist Government personnel with development of Statements of Work
  • Assist with technical evaluations and acquisition planning activities
  • Track contractor performance, deliverables, and invoice status
  • Monitor contract milestones and option periods
  • Support COR activities as requested
  • Support strategic planning initiatives
  • Analyze program performance and operational effectiveness
  • Develop recommendations for process improvements
  • Assist leadership with prioritization of future research initiatives
  • Support implementation of organizational best practices

Disclaimer: The above description is meant to illustrate the general nature of work and level of effort being performed by individuals assigned to this position or job description. This is not restricted as a complete list of all skills, responsibilities, duties, and/or assignments required. Individuals may be required to perform duties outside of their position, job description or responsibilities as needed.
The diversity of Axle's employees is a tremendous asset. We are firmly committed to providing equal opportunity in all aspects of employment and will not tolerate any illegal discrimination or harassment based on age, race, gender, religion, national origin, disability, marital status, covered veteran status, sexual orientation, status with respect to public assistance, and other characteristics protected under state, federal, or local law and to deter those who aid, abet, or induce discrimination or coerce others to discriminate.
Accessibility: If you need an accommodation as part of the employment process please contact: careers@axleinfo.com
This role has a market-competitive salary with an anticipated base compensation range listed below. Actual salaries will vary depending on a candidate's experience, qualifications, skills, and location.
Salary Range
$145,000-$155,000 USD