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

Clinical Research Coordinator

Vienna, VA

$24.25 - $32.25/hr

Who We Are DelRicht is a clinical research company dedicated to providing an excellent customer experience to all patients that participate in our clinical trials. Our clinical trials provide new ...

Research Associate - Equity Research B. Riley Securities | Arlington, VA Join a Top-Ranked Research Platform Where Your Impact Matters from Day One For more than 25 years, B. Riley Securities has ...

Research Associate

Arlington, VA ยท On-site

$80K - $100K/yr

Research Associate - Equity Research B. Riley Securities | Arlington, VA Join a Top-Ranked Research Platform Where Your Impact Matters from Day One For more than 25 years, B. Riley Securities has ...

Clinical Research Coordinator

Bethesda, MD ยท On-site

$26 - $34.50/hr

Job Title Clinical Research Coordinator Concentric Methods is seeking an experienced Clinical Research Coordinator to independently provide support services to the NIH. The total hourly pay for this ...

At Virginia Heart, we are looking for a professional Clinical Research Assistant plays a pivotal role in ensuring the smooth execution of clinical trials conducted at our site. As a vital member of ...

Clinical Research Coordinator

Leesburg, VA ยท On-site

$24.50 - $32.50/hr

At Virginia Heart, we are looking for a professional Clinical Research Coordinator will plan, direct, evaluate and analyze clinical research trials related to cardiac drug and device trials.

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 ...

Research Associate

Rockville, MD ยท 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 ...

Research Associate

Rockville, MD ยท 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 ...

Research Associate

Rockville, MD ยท 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 ...

Research Associate

Rockville, MD ยท 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 ...

Research Associate

Rockville, MD ยท 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 ...

Research Associate

Rockville, MD ยท 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 ...

Research Associate

Rockville, MD ยท 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 ...

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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 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 Coordinator III

Clinical Research Coordinator III

Alaka'ina Foundation Family of Companies

Silver Spring, MD โ€ข On-site

$25 - $33.25/hr

Full-time

Medical, Dental, Life, Retirement, PTO

Re-posted 20 days ago


Job description

Bering-Alaka`ina Holdings, LLC is looking for a Clinical Research Coordinator to support our government customer in Silver Spring, Maryland.
DESCRIPTION OF RESPONSIBILITIES:
  • Organize and prioritize all activities associated with conducting phase 1, 2, and 3 clinical and operational research studies within a military clinic setting.
  • Review and understand research protocols, ensuring applicable regulations, and guidelines are followed.
  • Coordinate space and supplies with appropriate personnel.
  • Recruit volunteers for the studies, to include determining volunteer population availability, advertising venues, and discussions with potential volunteers via telephone or e-mail.
  • Serve as a Volunteer advocate and associated duties.
  • Maintain study/test article accountability and administration.
  • Gather, prepare, and maintain appropriate information and documentation per applicable FDA regulations and ICH guidelines (e.g., source and case report forms, participant rosters, SOPs, etc.)
  • Enter required data on CRFs and audit records for accuracy, resolve discrepancies, and correct as necessary.
  • Coordinate with external and internal monitors.
  • Assist in training research staff on protocol-related study methods.
  • Monitor study data collection procedures to ensure uniformly high levels of compliance with GCP, GLP, FDA and other government- or locally-required guidances.
  • Able to design and create forms, reports, etc.
  • Maintain a safe workplace, observing appropriate safety and occupational health rules and regulations. Attend safety training relative to the position and report any infractions of safety procedures to the facility Safety Officer.
  • Other duties as assigned.

REQUIRED DEGREE/EDUCATION/CERTIFICATION:
  • Required to be a Registered Nurse licensed to practice in the state of Maryland, who are skilled and qualified in nursing procedures to include, but not limited to phlebotomy and the administration of experimental vaccines and other parenteral therapeutics as per specific protocol guidance in accordance with the 21 Code of Federal Regulation (CFR) 11, 50, 54, 56, 312, and 314.
  • Basic Life Support (BLS -CPR/AED) certification.
  • Maintain Certification in Clinical Research Coordination by Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA)

REQUIRED SKILLS AND EXPERIENCE:
  • Four (4) years clinical trials experience.
  • Five (5) years of experience in clinical research coordination, with expertise in FDA-regulated trials.
  • Experience facilitating clinical monitoring visits and resolving inquires.
  • Experience utilizing clinical trial management systems and databases (e.g., REDcap and Inform).
  • Must be able to work both independently and in a team setting.
  • Must have excellent communication, organization, and prioritization skills.
  • Intermittent physical activity including bending, reaching, and prolonged periods of sitting and or standing.
  • May be required to work at any facility and be responsible for own transportation.
  • Will be scheduled based on operational and business needs.
  • Required Knowledge, Skills and Abilities; knowledge of applicable highly complex scientific procedures and techniques relating to position.
  • Physical Capabilities: work may involve long periods of standing and handling of numerous chemicals and/or hazardous biological material.
  • Work Environment: Clinic/laboratory environment; may require working evenings and weekends.
  • Must be able to work independently and mentor other Clinic staff.
  • Must be able to work independently following a brief period of specific technical training.
  • Ability to establish and maintain effective working relationships with coworkers, managers and customers.

DESIRED SKILLS AND EXPERIENCE:
  • Advanced Cardiac Life Support (ACLS) certification encouraged.
  • Certification in clinical research (e.g., CCRP or CCRA) is preferred.
  • Commission for Case Manager Certification (CCMC) certification preferred.

REQUIRED CITIZENSHIP AND CLEARANCE:
A Tier I background investigation will be required.
Bering-Alaka`ina Holdings, LLC is a fast-growing government service provider. Employees enjoy competitive salaries. Eligible employees enjoy a 401K plan with company match; medical, dental, disability, and life insurance coverage; tuition reimbursement; paid time off; and 11 paid holidays.
We are an Equal Opportunity/Affirmative Action Employer of individuals with disabilities and veterans. We are proud to state that we do not illegally discriminate in employment decisions on the basis of any protected categories. If you are a person with a disability and you need an accommodation during the application process, please click here to request accommodation. We E-Verify all employees
"EOE, including Disability/Vets" OR "Equal Opportunity Employer, including Disability/Veterans"
Bering-Alaka`ina Holdings, LLC is comprised of industry-recognized government service firms designated as Alaska Native Corporation (ACN)-owned and 8(a) certified businesses and includes Ke`aki Technologies, LLC; Laulima Government Solutions, LLC; Kลซpono Government Services, LLC; Kapili Services, LLC; Po`okela Solutions, LLC; Kฤซkaha Solutions, LLC; and Pololei Solutions, LLC.
For additional information, please visit www.beringalakaina.com
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