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

System One

Research Associate

Rockville, MD · On-site

$28 - $43/hr

Research Associate Location : Rockville, MD Type: 6+ month Contract Pay Range: $28.00 - $43.00/hr Hours: Monday-Friday 9AM-5PM Overview Biopharmaceutical Company is seeking a Research Associate ...

System One Holdings, LLC

Research Associate

Rockville, MD · On-site

$28 - $43/hr

Research Associate Location : Rockville, MD Type: 6+ month Contract Pay Range: $28.00 - $43.00/hr Hours: Monday-Friday 9AM-5PM Overview Biopharmaceutical Company is seeking a Research Associate ...

System One

Research Associate

Rockville, MD · On-site

$28 - $43/hr

Research Associate Location : Rockville, MD Type: 6+ month Contract Pay Range: $28.00 - $43.00/hr Hours: Monday-Friday 9AM-5PM Overview Biopharmaceutical Company is seeking a Research Associate ...

The Democratic Party

Research Associate

Washington, DC · On-site

$54K/yr

The ideal Research Associate candidate should possess a basic understanding of the dynamic political climate and major policy issues in the U.S., as well as strong research and writing skills. If you ...

Trinityhealth

Clinical Research Coordinator

Silver Spring, MD · On-site

$25 - $33.25/hr

Clinical Research Coordinator Employment Type: Full-Time / 40 hours week Schedule/Shift: Day Shift Location: Silver Spring, Maryland with some travel to Germantown and practices required. Position ...

New

Trinity Health

Clinical Research Coordinator

Silver Spring, MD · On-site

$25 - $33.25/hr

Clinical Research Coordinator Employment Type: Full-Time / 40 hours week Schedule/Shift: Day Shift Location: Silver Spring, Maryland with some travel to Germantown and practices required. Position ...

New

Medix

Clinical Research Coordinator

Leesburg, VA · On-site

$35 - $36/hr

Support 5+ clinical research studies independently with minimal supervision. * Monitor study activities, maintain comprehensive regulatory files, and ensure adherence to protocols, FDA regulations ...

Hudson Institute

Research Associate

Washington, DC · On-site

$52K - $56K/yr

Description Hudson Institute seeks a research associate to support a senior fellow with their policy program focused on US national security, grand strategy, industrial policy, and defense industrial ...

ICON

Senior CRA

Washington, DC · On-site +1

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects ...

410 ICR United States USA

Senior CRA

Washington, DC · On-site

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects ...

New

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

Clinical Research Associate information

See Reston, VA salary details

$12

$42

$72

How much do clinical research associate jobs pay per hour?

As of Jul 18, 2026, the average hourly pay for clinical research associate 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.

Is it hard to get a CRA job?

Securing a Clinical Research Associate (CRA) position can be competitive, often requiring relevant education such as a degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certifications like CCRP can improve job prospects, but entry may still be challenging for those without prior experience or specialized training.

What are Clinical Research Associates?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate, and why are they important?

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

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

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

What is the work of clinical research associate?

A clinical research associate (CRA) monitors clinical trials to ensure they are conducted according to protocols, regulations, and Good Clinical Practice standards. They coordinate with investigators, review trial data, and ensure compliance, often using clinical trial management systems. CRAs typically require knowledge of regulatory requirements and may need certification or training in clinical research.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically an entry-level to mid-level position in clinical research, often requiring a bachelor's degree in a related field and some experience or training in clinical trials. Entry-level CRAs may need to complete training on Good Clinical Practice (GCP) and may start as clinical trial assistants or coordinators before advancing to CRA roles.

How do you become a clinical research associate?

To become a clinical research associate (CRA), candidates typically need a bachelor's degree in a health-related field such as life sciences, nursing, or pharmacy. Relevant experience in clinical trials, knowledge of Good Clinical Practice (GCP), and certification from organizations like the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) can enhance job prospects. CRAs often undergo on-the-job training and may pursue additional certifications to advance their careers.

What are some common challenges Clinical Research Associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.
More about Clinical Research Associate jobs
What are the most commonly searched types of Clinical Research jobs in Reston, VA? The most popular types of Clinical Research jobs in Reston, VA are:
What are popular job titles related to Clinical Research Associate jobs in Reston, VA? For Clinical Research Associate jobs in Reston, VA, the most frequently searched job titles are:
What job categories do people searching Clinical Research Associate jobs in Reston, VA look for? The top searched job categories for Clinical Research Associate jobs in Reston, VA are:
What cities near Reston, VA are hiring for Clinical Research Associate jobs? Cities near Reston, VA with the most Clinical Research Associate job openings:
Clinical Research Associate jobs near you
Research Associate

Research Associate

System One

Rockville, MD • On-site

$28 - $43/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted yesterday

Job description

Job Title: Research Associate Location: Rockville, MD Type: 6+ month Contract Pay Range: $28.00 - $43.00/hr Hours: Monday-Friday 9AM-5PM

Overview Biopharmaceutical Company is seeking a Research Associate, working with animal modeling to support the R&D of cancer treatment therapies! Responsibilities

  • Assay and Data Management: Perform various assays, tests, and studies related to animal modeling. Calculate and analyze raw data to complete research test results. Collate data, perform statistical analyses using software tools such as Microsoft Office, GraphPad Prism, and R Studio. Maintain detailed notes and log data in computer databases and laboratory notebooks.
  • Mammalian Cell Culture: Oversee all aspects of mammalian cell culture, including media and buffer preparation, culture initiation, propagation, and cryopreservation. Handle primary human cells from commercial and patient sources. Ensure that all cell culture procedures are conducted according to standard operating procedures.
  • Flow Cytometry: Assess target antigen expression using traditional and spectral flow cytometry techniques on various in-vitro and ex-vivo samples. Prepare and process samples for cytometric analysis.
  • Dosing Formulations and Reporting: Prepare dosing formulations for in-vivo studies. Report experimental results to the supervisor and collaborate with investigators. Ensure timely and accurate documentation of experimental protocols and data.
  • Record Keeping and Compliance: Maintain detailed and accurate records of experimental data and procedures in laboratory notebooks. Adhere to standard operating procedures and ensure compliance with all regulatory requirements.

Requirements

  • Bachelor's Degree in Animal Science, Biology, or related science field
  • 2+ years of tissue culture, traditional and spectral flow cytometry, animal handling experience (for imaging) and IVIS imaging
  • Strong computer skills, including proficiency with basic data analysis programs (Microsoft Office, GraphPad Prism, Pristima, etc.) and programming and data analysis (R Studio, Linux, etc.)

System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#M-3 #LI-GS1 Ref: #558-Scientific

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