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Clinical Research Associate Cro Jobs in Reston, VA

Emmes

Sr. Clinical Research Associate

Rockville, MD · Hybrid

Through our two business units- Emmes, a full-service CRO , and Veridix AI, our technology, data ... The Senior Clinical Research Associate (CRA) is responsible for monitoring clinical study sites ...

Icon plc

Clinical Research Associate

Washington, DC · On-site

$91K - $114K/yr

Clinical Research Associate - Multi Therapeutic Area (Early Development) - West Region ICON is a ... CRO industry * Experienced monitoring early development Phase I/II clinical studies, across ...

Medix

Clinical Research Coordinator

Bethesda, MD · Hybrid

About this role: - Hybrid 2 Days onsite & 3 Days Remote - Must have CRO experience!!!! The In-House Clinical Research Associate is responsible for supporting clinical study teams, primarily the field ...

New

Emmes

Clinical Research Associate I

Rockville, MD

Through our two business units- Emmes, a full-service CRO , and Veridix AI, our technology, data ... The Clinical Research Associate (CRA) I is responsible for monitoring clinical study sites either ...

Emmes

Clinical Research Associate II

Rockville, MD · Hybrid

Through our two business units- Emmes, a full-service CRO , and Veridix AI, our technology, data ... The Clinical Research Associate (CRA) II is responsible for monitoring clinical study sites either ...

Emmes

Senior Clinical Research Associate

Rockville, MD · On-site +1

Overview Senior Clinical Research Associate US remotely and on-site (80% travel) Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research ...

ICON

Senior Clinical Research Associate

Washington, DC · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Washington DC ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Icon plc

Senior Clinical Research Associate

Washington, DC · Hybrid

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Washington DC ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Icon plc

Clinical Research Associate

Washington, DC · On-site

$91K - $114K/yr

Clinical Research Associate - West Coast ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...

Icon plc

Clinical Research Associate

Washington, DC · On-site

$91K - $114K/yr

Clinical Research Associate - Early Stage Development - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

Emmes

Clinical Research Associate II

Rockville, MD · On-site +1

Overview Clinical Research Associate II US remotely and on-site (80% travel) Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing ...

Kelly Services

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

Coordinate multiple clinical research studies simultaneously from study startup through final ... Serve as the primary operational contact during monitoring visits, facilitating sponsor, CRO ...

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All JobsClinical Research Associate Cro JobsClinical Research Associate Cro Jobs in Reston, VA

Clinical Research Associate Cro information

See Reston, VA salary details

$12

$42

$72

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

As of Aug 7, 2026, the average hourly pay for clinical research associate cro in Reston, VA is $42.79, according to ZipRecruiter salary data. Most workers in this role earn between $30.00 and $54.76 per hour, depending on experience, location, and employer.

What is the difference between Clinical Research Associate Cro vs Clinical Trial Assistant?

AspectClinical Research Associate CroClinical Trial Assistant
CredentialsBachelor's degree, often with certifications like CCRP or RACTypically a high school diploma or associate degree, with some roles requiring a certificate
Work EnvironmentConducts site visits, monitors trials, and ensures complianceSupports trial coordination, manages documentation, and assists with logistics
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, CROs, clinical trial teams

The Clinical Research Associate Cro focuses on monitoring clinical trials, ensuring compliance, and site management. In contrast, the Clinical Trial Assistant provides administrative support, manages documentation, and assists with trial logistics. Both roles are essential in clinical research but differ in responsibilities and required experience.

What are popular job titles related to Clinical Research Associate Cro jobs in Reston, VA? For Clinical Research Associate Cro jobs in Reston, VA, the most frequently searched job titles are:
What job categories do people searching Clinical Research Associate Cro jobs in Reston, VA look for? The top searched job categories for Clinical Research Associate Cro jobs in Reston, VA are:
What cities near Reston, VA are hiring for Clinical Research Associate Cro jobs? Cities near Reston, VA with the most Clinical Research Associate Cro job openings:
Clinical Research Associate Cro jobs near you
Infographic showing various Clinical Research Associate Cro job openings in Reston, VA as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $88,994 per year, or $42.8 per hour.

Sr. Clinical Research Associate

Icon plc

Washington, DC

$110K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 28 days ago

Job description

Senior Clinical Research Associate - Oncology (Myelofibrosis) - West Region

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


What You Will Be Doing:

  • Serve as the primary point of contact between investigational sites and the sponsor

  • Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out

  • Ensure site compliance with ICH-GCP, SOPs, and regulations

  • Maintain up-to-date documentation in CTMS and eTMF systems

  • Support and track site staff training and maintain compliance records

  • Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting

  • Support subject recruitment and retention efforts at the site level

  • Oversee drug accountability and ensure proper storage, return, or destruction

  • Resolve data queries and drive timely, high-quality data entry

  • Document site progress and escalate risks or issues to the clinical team

  • Assist in tracking site budgets and ensuring timely site payments (as applicable)

  • Collaborate with cross-functional partners including CTAs, LTMs, and CTMs

You are:

  • A graduate with a Bachelor's degree in Life Sciences or equivalent, or a qualified RN

  • Eligible to work in United States without visa sponsorship

  • A clinical research professional with 3+ years of on-site monitoring experience in the pharmaceutical or CRO industry

  • Experienced monitoring Oncology specifically Myelofibrosis clinical trials.

  • Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF

  • A clear communicator, problem-solver, and collaborative team player

  • Willing and able to travel up to 50% for on-site monitoring visits across the West region; preference given to candidates residing near major HUB airport to support efficient regional travel.


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Salary Range

$110,520.00-$138,150.00

Are you a current ICON Employee? Please click here to apply

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