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Clinical Research Manager Jobs in Virginia (NOW HIRING)

Alcanza Clinical Research

$23.50 - $31.25/hr

The Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes ...

Tekton Research Inc

Clinical Research Coordinator

Richmond, VA · On-site

$22.50 - $29.75/hr

Clinical Research Coordinator (CRC) About Tekton Research: Tekton Research is a growth-oriented ... Coordinate and manage all aspects of assigned clinical trials from study start-up through close-out.

Tekton Research Inc

Clinical Research Coordinator

Richmond, VA · On-site

$22.50 - $29.75/hr

Clinical Research Coordinator (CRC) About Tekton Research: Tekton Research is a growth-oriented ... Coordinate and manage all aspects of assigned clinical trials from study start-up through close-out.

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Clinical Research Manager information

See Virginia salary details

$48.6K

$106.4K

$187.4K

How much do clinical research manager jobs pay per year?

As of Sep 3, 2026, the average yearly pay for clinical research manager in Virginia is $106,415.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,300.00 and $121,400.00 per year, depending on experience, location, and employer.

What does a clinical research manager do?

A clinical research manager oversees clinical trials, which involve testing new medications or medical devices. Their responsibilities include ensuring all ethical practices and legal protocols are followed and that all paperwork is filled out completely and accurately. They also maintain standards for the data collection and procedures during the clinical trial and make sure all team members, including the doctors and nurses on the trial, are kept informed.

What are the key skills and qualifications needed to thrive as a clinical research manager?

To thrive as a Clinical Research Manager, you need a solid understanding of clinical trial protocols, regulatory requirements (such as GCP), and a background in life sciences or healthcare, often supported by a relevant degree. Familiarity with clinical trial management systems (CTMS), EDC software, and certifications like ACRP or SOCRA are typically expected. Strong leadership, excellent organizational skills, and effective communication abilities set outstanding managers apart. These competencies are critical for ensuring compliance, data integrity, and the successful coordination of multidisciplinary research teams.

What are some common challenges clinical research managers face when overseeing multiple clinical trials simultaneously?

Clinical Research Managers often encounter challenges such as balancing competing timelines, ensuring regulatory compliance across different studies, and effectively allocating resources among projects. Managing communication between diverse teams—such as investigators, sponsors, and regulatory bodies—can also be demanding, especially when trials are at different stages. Developing strong organizational skills and leveraging project management tools are key to successfully navigating these complexities and maintaining high standards for data quality and participant safety.

What is the difference between Clinical Research Manager vs Clinical Research Coordinator?

AspectClinical Research ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with experience in project managementBachelor's in health sciences or related field, often with certification like CCRP
Work EnvironmentOversees multiple studies, manages teams, and ensures compliance at a higher levelAssists with daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites

The Clinical Research Manager focuses on overseeing entire studies and managing teams, while the Clinical Research Coordinator handles daily study tasks and participant interactions. Both roles require relevant certifications and are essential in clinical research settings, but they differ in scope and responsibilities.

More about Clinical Research Manager 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 Manager jobs in Virginia?

For Clinical Research Manager jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Clinical Research Manager jobs in Virginia look for?

The top searched job categories for Clinical Research Manager jobs in Virginia are:

What cities in Virginia are hiring for Clinical Research Manager jobs?

Cities in Virginia with the most Clinical Research Manager job openings:

Clinical Research Manager jobs near you
Infographic showing various Clinical Research Manager job openings in Virginia as of August 2026, with employment types broken down into 3% As Needed, 86% Full Time, 5% Part Time, 3% Temporary, and 3% Contract. Highlights an 97% In-person, and 3% Remote job distribution, with an average salary of $106,415 per year, or $51.2 per hour.

Regional Manager, Clinical Research (32366)

GI Alliance

Alexandria, VA • On-site

Full-time

Posted 5 days ago

Key responsibilities

  • Coordinate and oversee clinical trials at 3-4 research site locations within a designated region.

  • Lead and support research staff, including training, delegation, hiring, and performance reviews.

  • Assist with patient recruitment, trial setup, site qualification, monitoring, and documentation management.

GI Alliance rating

6.4

Company rating: 6.4 out of 10

Based on 69 frontline employees who took The Breakroom Quiz

650th of 898 rated healthcare providers

Job description

JOB DESCRIPTION
JOB TITLE: Regional Clinical Research Manager
FSLA STATUS: Exempt
POSITION SUMMARY:
The Regional Clinical Research Manager is responsible for the coordination and administration of clinical trials at 3-4 clinical research site locations within a designated region under the direction of the VP of Operations and Director of Research Strategy and Operations. They are responsible for overseeing clinical research staff to ensure the successful conduct of clinical trials, and ensuring compliance with established regulations and standards.
JOB RELATIONSHIPS:
  • Reports directly to the Director of Strategy and Operations and indirectly to the Urology America leadership. This role is also responsible to the individual market presidents, the Principal Investigators of each trial, and the physician partners of each practice.
  • Collaborates with clinical providers, local vendors, site staff, clinic patient navigators, IT, and data management.

ROLE QUALIFICATIONS: (experience, education, and skills)
  • Must have ≥ 5 yrs experience with conducting clinical trials.
  • Urology based clinical research experience highly preferred.
  • Held previous leadership roles within an organization.
  • Bachelor's degree in a health or science field preferred.
  • Experience with overseeing and conducting pharmaceutical and device study protocols.
  • Must have knowledge of and experience with GCPs and relevant federal and state regulatory guidelines.
  • Excellence in computer software including Microsoft Office Suite, EMR, Practice Management, Electronic Data Capture (EDC), and Clinical Trail Management Systems (CTMS).
  • Exceptional time management skills and the ability to prioritize work.
  • Excellent communication skills and the ability to interact with all levels of management, staff, sponsors, and providers.

ESSENTIAL JOB RESPONSIBLITIES:
Work to build and manage research departments in scope, size, reputation, and professionalism and works to accomplish this in all locations and markets assigned.
  • Leads research department staff by conducting training, assigns delegation of responsibilities, supports staff hiring, and manages yearly staff reviews, etc. Oversight and support of CRCs in all markets is a primary responsibility of this role.
  • Assists with patient recruitment for studies, review protocols, completion and submission of feasibility documents, leads trial set-up and launch, plans for and oversees site qualification, initiation, monitoring, audit visits, etc. Supports these endeavors in all locations and markets assigned.
  • Maintain relevant certifications in, and continually update knowledge of, FDA, GCP, ICH, federal and state regulations, etc. Provide relevant updates to other research staff as applicable.
  • Works closely with the IRB/Recruitment Specialist to ensure timely submissions, updates, close-outs, etc.
  • Responsible for maintenance of accurate and complete documentation, primarily executed by the CRCs, including but not limited to regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, subject logs, and study-related communications.
  • Design, implement, and manage system for organizing, planning, and controlling workflow related to all clinical research activities.
  • Work with the EMR and data management systems to complete/monitor completion of EDC, eCRFs, adverse event documentation, maintain patient records, create strategies for patient recruitment.
  • Assist CRCs with identification and prompt reporting of protocol deviations, AEs, and SAEs in accordance with protocol, IRB, and/or sponsor requirements
  • Work closely with IRB, study sponsors, PIs and Sub-Is. Attend necessary meetings and calls.
  • Provide continuous communication on study conduct, pre-study through post-study to all relevant stakeholders, including internal communication regarding enrollment, progress, and completion of trials.
  • Monitor invoicing, billing, and payments, in collaboration with the finance department to ensure timely and accurate A/R process.
  • Create, review, and maintain staff CVs, certifications, etc.
  • Evaluate, purchase, maintain necessary equipment and equipment monitoring.
  • Participate in site visits, SIVs, monitoring, etc.
  • Work directly with patients to support CRCs in screening, consenting, history taking, completing necessary exams including EKG, blood draw, vitals, procedure visits, etc.
  • Complete necessary study close-out steps and documentation.
  • Prepares for and participates in FDA inspections.
  • Communicate with and support patients and their families as necessary.
  • Maintain HIPAA compliant communication and confidentiality, at all times.
  • Assist with other duties assigned.
  • Acts as primary liaison to local market clinic and research department.

Performance Requirements:
Knowledge
  • Knowledge of clinical research in a specialty setting; medical practice clinical and administrative systems, clinical research software, and sponsor requirements for successful clinical trial completion.
  • Understanding of medical terminology.

Skills
  • Ability to use multi-line phone systems and relevant computer systems.
  • Interpersonal and communication both with internal staff and external customers.
  • Skill in evaluating and implementing study protocols and budgets.
  • Skill in reading medical chart terminology.
  • Time Management.

Abilities
  • Ability to communicate effectively with patients, staff, and external contacts via phone, in person, and through electronic mail.
  • Elicit appropriate information for patients to clinic staff.
  • Ability to read and understand information and ideas presented in writing.
  • Ability to apply general rules to specific problems to produce answers that make sense - deductive reasoning.

Travel
  • 25-50 % travel to regional sites assigned

Reporting to this position: CRC/Operations Leads, Clinical Research Coordinators, Clinical Research Assistants, Interns, other research staff as department grows
Physical Demands and Work Environment:
The physical demands and work environment characteristics described here are the representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions:
  • Physical demands: Involves sitting approximately 70-90 percent of the day, walking or standing for the remainder. Work may require stooping and bending, mobility to complete patient study visits, and lifting up to 25 pounds.
  • Work environment: Primarily office setting, with time in the clinical setting for patient study visits. Noise level in the work environment is usually moderate. Clean, well-lighted office/clinical environment. Will require travel between Urology Austin clinical locations and outside Ambulatory Surgery Centers (ASC) to meet study demands.

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