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Clinical Research Operations Manager Jobs in Virginia

Virginia Heart

Clinical Research Coordinator

Leesburg, VA

$24.50 - $32.50/hr

Participates in preparation and management of research budgets and monetary disbursements ... Clinical experience preferred * Certified Clinical Research Coordinator (CCRC) or Certified ...

Galen College of Nursing

Research Nurse

Richmond, VA · On-site

Apprises principal investigator, Research Operations Director and Regional Site Manager of all ... Computer skills including use of clinical trial database, electronic data capture, and MS Word or ...

New

Mission Hospital

Research Nurse

Richmond, VA · On-site

$69K - $103K/yr

Apprises principal investigator, Research Operations Director and Regional Site Manager of all ... Computer skills including use of clinical trial database, electronic data capture, and MS Word or ...

New

Catholic Medical Center

Research Nurse

Richmond, VA · On-site

Apprises principal investigator, Research Operations Director and Regional Site Manager of all ... Computer skills including use of clinical trial database, electronic data capture, and MS Word or ...

New

PRISM Vision Group

Clinical Research Nurse

Hampton, VA · On-site

$47K - $128K/yr

Clinical Research RN Opportunity Virginia Oncology Associates, the largest group of medical ... Experience with computer data entry and database management * Excellent written and oral ...

New

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Clinical Research Operations Manager information

See Virginia salary details

$34.7K

$97.2K

$184.9K

How much do clinical research operations manager jobs pay per year?

As of Aug 9, 2026, the average yearly pay for clinical research operations manager in Virginia is $97,198.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,900.00 and $112,500.00 per year, depending on experience, location, and employer.

How does a clinical research operations manager collaborate with cross-functional teams during a study?

As a Clinical Research Operations Manager, you will work closely with cross-functional teams including clinical trial coordinators, data managers, regulatory affairs specialists, and principal investigators. Your role involves facilitating clear communication between departments, ensuring that study milestones are met, and resolving operational issues as they arise. Regular meetings and status updates are common, and you'll often act as a liaison to keep all stakeholders aligned on study objectives, timelines, and compliance requirements. This collaborative approach is crucial for maintaining study integrity and ensuring successful trial outcomes.

What does a clinical research operations manager do?

A Clinical Research Operations Manager oversees the daily operations of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. They coordinate between research staff, sponsors, and regulatory bodies, manage budgets and timelines, and ensure proper documentation and reporting. Their role is essential in maintaining the quality and integrity of clinical studies from start to finish.

What are the key skills and qualifications needed to thrive as a clinical research operations manager, and why are they important?

To thrive as a Clinical Research Operations Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications such as ACRP or SOCRA are highly valuable. Leadership, problem-solving, and excellent organizational and communication skills help you manage teams and collaborate effectively with stakeholders. These skills and qualities are crucial for ensuring the successful execution of clinical trials while maintaining regulatory standards and operational efficiency.
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Clinical Research Operations Manager jobs near you
Infographic showing various Clinical Research Operations Manager job openings in Virginia as of August 2026, with employment types broken down into 85% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $97,198 per year, or $46.7 per hour.

Clinical Research Assistant (3032) - Clinical Research

Tidewater Physicians Multispecialty Group

Williamsburg, VA • On-site

Full-time

Re-posted 8 days ago

Job description

Tidewater Physicians Multispecialty Group is actively seeking a Clinical Research Assistant to work for our Clinical Research office in Williamsburg. Tidewater Physicians Multispecialty Group (TPMG) is comprised of over 200 physicians and advanced practice clinicians, and is the largest physician-owned group on the Peninsula. The schedule is full-time, 8a.m. to 5p.m. Monday through Friday with flexibility as determined after onboarding and training are complete.
Position Summary
Clinical Research Assistant will report directly to the Clinical Research Coordinator and be responsible for performing assigned duties, to include, but not limited to, data mining, data entry and presentation. Candidates with experience working in a research setting are a plus, but not required. A knowledge of medical terminology is helpful.

Major Duties and Responsibilities
  • Assess eligibility of potential subjects through review of medical records and discussion of patient status with the Medical Director, the Principal Investigator, other Investigators, nurses and/or the CRC as appropriate.
  • Collect, maintain and enter data in keeping with the requirements of the department and the particular study as required; this may be electronic or printed based on requirements of the study.
  • Assist the CRC in the performance of other study related duties and general office support as instructed.
  • Other duties as assigned.
Knowledge, Skills and Abilities
  • Knowledge of medical terminology to include symptomology, diagnoses, medications, anatomy and standard medical equipment and procedures is helpful, but not required.
  • Ability to work scheduled hours as defined in the job offer. Must be able to work flexible hours
  • Must have excellent interpersonal skills with staff and all health care professionals with excellent verbal and written communication skills, consistent professional conduct, and meticulous attention to detail.
  • Must become familiar with the Clinical Research department’s SOP’s and study protocols, and is responsible for following these.
EDUCATION/TRAINING/REQUIREMENTS
  • Experience in healthcare preferred.
  • Experience with EHR preferred.
  • Previous experience with clinical trials a plus.
PHYSICAL DEMANDS
  • Ability to stand and walk for long periods of time.
  • Ability to sit for extended periods of time.
  • Ability to grasp and hold up to 25 lbs.*
  • Ability to hear normal voice level communications in person or through the telephone.
  • Ability to speak clearly and understandably.
SUCCESS FACTORS
  • Excellent Time Management/Organized
  • Open Communication/Positive
  • Goal Driven
  • Excellent Customer Service
  • Juggles Multiple Priorities
  • Accuracy and Attention to Detail
  • Accomplished in word processing and worksheet utilization
Come join the TPMG team!
TPMG is an equal opportunity employer committed to a diverse and inclusive workforce.

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