Clinical Research Coordinator
The Voluntary Protection Programs Participants' Association, Inc, Portsmouth, VA, United States
About the Opportunity
FHR Solutions has been engaged to support a search for a leading clinical research company seeking a
Clinical Research Coordinator (CRC) . This is an exciting opportunity to contribute to impactful clinical studies in a structured, compliance-driven research environment. The role involves coordinating clinical trials, ensuring protocol adherence, and maintaining high standards of data integrity and participant safety.
Role Summary
The Clinical Research Coordinator is responsible for the day-to-day operational management of clinical research studies. This includes site communication, participant screening support, data oversight, regulatory documentation, and protocol compliance. The role involves working closely with study teams and participants, including military personnel, veterans, and beneficiaries, within a Department of Defense (DoD) healthcare environment.
Key Responsibilities
Coordinate operational aspects of clinical research projects across assigned study sites.
Support the development, maintenance, and review of regulatory documents (e.g., ICFs, protocol amendments, IRB submissions).
Assist in participant screening, eligibility verification, recruitment tracking, and scheduling.
Serve as a point of contact for site personnel, investigators, and DoD clinical research offices.
Ensure all study activities comply with Good Clinical Practice (GCP), FDA, ICH, and DoD Human Research Protection Program (HRPP) requirements.
Support data abstraction from Military Health Systems and accurate entry into Electronic Data Capture (EDC) systems.
Monitor protocol adherence and escalate deviations or safety concerns appropriately.
Prepare for site visits, audits, and monitoring activities.
Collaborate with cross-functional stakeholders, including biostatistics, data science, and clinical operations teams.
Maintain complete study records, logs, and documentation in compliance with organizational SOPs and DoD regulations.
Perform protocol procedures as needed (e.g., phlebotomy, ECGs, biological specimen collection).
Required Qualifications
Bachelor’s degree in science, public health, healthcare administration, or related field.
Minimum of 5 years of clinical research experience.
Ability to obtain and maintain a Secret Security Clearance per DoD requirements.
Highly Desired
SOCRA or ACRP certification.
Experience in DoD, VA, or Federal Healthcare settings.
Strong knowledge of GCP.
Experience with Electronic Health Record (EHR) systems such as MHS GENESIS (Cerner).
If you thrive in structured, compliance-driven research environments and want to support meaningful studies, we’d love to connect.
Pay: $65,000.00 - $85,000.00 per year
Work Location: In person
#J-18808-Ljbffr
FHR Solutions has been engaged to support a search for a leading clinical research company seeking a
Clinical Research Coordinator (CRC) . This is an exciting opportunity to contribute to impactful clinical studies in a structured, compliance-driven research environment. The role involves coordinating clinical trials, ensuring protocol adherence, and maintaining high standards of data integrity and participant safety.
Role Summary
The Clinical Research Coordinator is responsible for the day-to-day operational management of clinical research studies. This includes site communication, participant screening support, data oversight, regulatory documentation, and protocol compliance. The role involves working closely with study teams and participants, including military personnel, veterans, and beneficiaries, within a Department of Defense (DoD) healthcare environment.
Key Responsibilities
Coordinate operational aspects of clinical research projects across assigned study sites.
Support the development, maintenance, and review of regulatory documents (e.g., ICFs, protocol amendments, IRB submissions).
Assist in participant screening, eligibility verification, recruitment tracking, and scheduling.
Serve as a point of contact for site personnel, investigators, and DoD clinical research offices.
Ensure all study activities comply with Good Clinical Practice (GCP), FDA, ICH, and DoD Human Research Protection Program (HRPP) requirements.
Support data abstraction from Military Health Systems and accurate entry into Electronic Data Capture (EDC) systems.
Monitor protocol adherence and escalate deviations or safety concerns appropriately.
Prepare for site visits, audits, and monitoring activities.
Collaborate with cross-functional stakeholders, including biostatistics, data science, and clinical operations teams.
Maintain complete study records, logs, and documentation in compliance with organizational SOPs and DoD regulations.
Perform protocol procedures as needed (e.g., phlebotomy, ECGs, biological specimen collection).
Required Qualifications
Bachelor’s degree in science, public health, healthcare administration, or related field.
Minimum of 5 years of clinical research experience.
Ability to obtain and maintain a Secret Security Clearance per DoD requirements.
Highly Desired
SOCRA or ACRP certification.
Experience in DoD, VA, or Federal Healthcare settings.
Strong knowledge of GCP.
Experience with Electronic Health Record (EHR) systems such as MHS GENESIS (Cerner).
If you thrive in structured, compliance-driven research environments and want to support meaningful studies, we’d love to connect.
Pay: $65,000.00 - $85,000.00 per year
Work Location: In person
#J-18808-Ljbffr