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Clinical Research Associate Jobs in Virginia (NOW HIRING)

Virginia Heart

Clinical Research Coordinator

Leesburg, VA

$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.

Virginia Tech

Research Associate

Blacksburg, VA · On-site

Research Associate Apply now Back to search results Job no: 536733 Work type: Research Faculty Senior management: Vice President for Research Department: Fralin Biomedical Res. Institute Location:

Dinte Executive Search

Research Associate

Mclean, VA · On-site

Qualifications An ideal candidate has a solid liberal arts academic record, is passionate about research and writing, and has strong analytical skills. The Associate will have a consultative approach ...

Dinte Executive Search

Research Associate

Mclean, VA

Qualifications An ideal candidate has a solid liberal arts academic record, is passionate about research and writing, and has strong analytical skills. The Associate will have a consultative approach ...

ObjectiveHealth

Clinical Research Coordinator II

Richmond, VA · On-site

$22.25 - $29.75/hr

Description Clinical Research Coordinator II Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator II. The ideal candidate ...

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Clinical Research Associate information

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How much do clinical research associate jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for clinical research associate in Virginia is $40.77, according to ZipRecruiter salary data. Most workers in this role earn between $28.61 and $52.21 per hour, depending on experience, location, and employer.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree such as a life sciences or healthcare-related field, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with clinical trial management systems can improve job prospects, but entry may be challenging for those without relevant qualifications or experience.

What is a clinical research associate?

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?

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.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and the chance to contribute to medical advancements, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in healthcare and research.

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 Virginia? The most popular types of Clinical Research jobs in Virginia are:
What are popular job titles related to Clinical Research Associate jobs in Virginia? For Clinical Research Associate jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Clinical Research Associate jobs in Virginia look for? The top searched job categories for Clinical Research Associate jobs in Virginia are:
What cities in Virginia are hiring for Clinical Research Associate jobs? Cities in Virginia with the most Clinical Research Associate job openings:
Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Virginia as of August 2026, with employment types broken down into 2% As Needed, 69% Full Time, 21% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $84,808 per year, or $40.8 per hour.

Clinical Research Coordinator

Eastern Virginia Medical School

Norfolk, VA • On-site

$73K/yr

Full-time

Re-posted 13 days ago

Job description

Overview
The primary responsibility of the Clinical Research Coordinator is to coordinate the day-to-day administrative and operational logistics of assigned clinical trials. The Clinical Research Coordinator is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As the primary resource for the protocols, the Clinical Research Coordinator will act as liaison between the investigators, primary care providers, the institutional review board (IRB), and the sponsor. Along with the investigator, the Clinical Research Coordinator will screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, the Clinical Research Coordinator is responsible for all data and source documentation, adverse experience reporting, and maintenance of complete regulatory files.
Please note, this position is coterminous with grant funding.
Responsibilities
  • Possess a sound and in-depth understanding of each study protocol that has been assigned as a primary responsibility. Review with the principal investigator and other study staff the inclusion/exclusion criteria, overall structure, and requirements of each protocol. Serve as the main point of contact with the study sponsors. Attend study-related meetings as appropriate. Coordinate the activities of various research team members to ensure completion of study objectives.
  • Develop a mechanism for subject recruitment and ongoing communications with primary care physicians and study staff, as appropriate. The coordinator reviews all eligibility requirements with the study participant and reports this to the Principal Investigator, who makes the final eligibility approval. Schedule subjects for screenings and follow-up visits. Maintain telephone contact with subjects in between visits, as needed.
  • Review the protocol, informed consent form, and follow-up procedures with potential study subjects. Ensure the subject understands the study prior to signing the consent form ensure the current approved informed consent is signed before subjects are screened and enrolled. Develop and distribute study materials to participants as needed.
  • Ensure appropriate specimen collection. Experience with phlebotomy and processing/shipping of specimens highly desired. Review laboratory data and communicate abnormal values to the primary care provider and investigator for final sign off.
  • Provide maintenance of medication/drug inventory/storage as well as investigational product accountability/dispensation logs. Coordinator will document and report all noted adverse events as well as notifying the study sponsor and/or site investigator.
  • Ensure adherence to protocol requirements and that the randomization procedure is followed as per protocol guidelines. Document protocol exemptions and deviations, as appropriate.
  • Assess and record all adverse events as outlined in protocol. Report all serious adverse events to the principal investigator, sponsor's monitor, primary care physician, and IRB as outlined in the protocol. Communicate regularly with the principal investigator about study-related issues.
  • Submit all study materials to the appropriate IRB for approval. Submit amendments, continuing review reports and adverse events to the IRB.
  • Maintain source documentation for all CRF entries, including clinic chart visit notes, lab data, and procedure reports. Ensure timely and accurate case report form (CRF) completion for each study subject and provide auditors with completed CRFs, medical records, lab data and other source documents for review. Maintain copies of all required regulatory documents in an organized manner.
  • Complete and pass the required courses/tests/certificates and human subjects/ethics training courses.

Qualifications
Minimum Qualifications and Skills:
  • Bachelor's degree or an equivalent combination of education, training, and relevant experience.
  • Three (3) years of experience in clinical research protocols
  • Previous experience with clinical research protocols preferred. Ability to think and work independently, insight, excellent organizational skills, astute and accurate patient assessment skills, and the ability to identify and assign priorities.

Preferred Qualifications:
  • Experience in cognitive impairment/dementia research highly desired
  • Five (5) years of clinical research experience

Location : Location
US-VA-Norfolk

Apply