Azimuth Research Group is a life sciences research firm that leverages point-of-care data to address complex challenges for clients in the pharmaceutical, biotechnology, and academic sectors. Our vision is to transform the research landscape by embedding continuous, adaptive research into healthcare delivery ecosystems.
Location: Portsmouth, VA (Onsite)
Position Overview
Azimuth Research Group is seeking two full-time, on-site professionals to support clinical research operations within a Department of Defense (DoD) healthcare environment.
- Clinical Research Nurse (CRN)
- Clinical Research Coordinator (CRC)
Both roles play a critical part in executing clinical studies involving active-duty service members, veterans, and beneficiaries. These positions require strong clinical or research expertise, regulatory knowledge, and the ability to thrive in a structured, compliance-driven environment.
Clinical Research Nurse (CRN)
The Clinical Research Nurse combines direct patient care with protocol-driven clinical research execution. This role requires advanced clinical judgment, regulatory awareness, and strong collaboration across multidisciplinary teams.
Key Responsibilities
- Conduct clinical assessments, vital signs, and study procedures within scope of nursing practice
- Administer investigational products (as permitted) and monitor participants
- Support participant recruitment, screening, and informed consent
- Ensure compliance with GCP, FDA, ICH, and DoD Human Research Protection Program (HRPP) requirements
- Maintain accurate clinical documentation and support EDC query resolution
- Serve as a liaison between clinicians, research teams, and military personnel
- Support protocol adherence, deviation reporting, and audit readiness
- Collaborate with CRCs on regulatory documentation and study logistics
- Perform protocol procedures (e.g., phlebotomy, ECGs, specimen collection)
Required Qualifications
- Bachelor of Science in Nursing (BSN)
- Minimum 2 years of clinical nursing experience
- Ability to obtain and maintain Secret Security Clearance (DoD requirement)
- Strong clinical assessment and documentation skills
Highly Desired
- ACRP or SOCRA certification
- Knowledge of Good Clinical Practice (GCP)
- Experience with MHS GENESIS
- Experience in DoD, VA, or federal healthcare environments
Clinical Research Coordinator (CRC)
The Clinical Research Coordinator is responsible for the day-to-day coordination of clinical trials, ensuring operational excellence, regulatory compliance, and data integrity across study activities in a DoD healthcare setting.
Key Responsibilities
- Coordinate operational aspects of clinical research studies across assigned sites, including military treatment facilities
- Develop, maintain, and review regulatory documentation (e.g., ICFs, protocol amendments, IRB submissions)
- Support participant screening, eligibility verification, recruitment tracking, and scheduling
- Serve as a primary point of contact for site personnel, investigators, and DoD research offices
- Ensure compliance with GCP, FDA, ICH, and DoD HRPP requirements
- Perform data abstraction from Military Health Systems and ensure accurate entry into EDC systems
- Monitor protocol adherence and elevate deviations or safety concerns
- Support site visits, audits, and monitoring activities, including follow-up documentation
- Collaborate with cross-functional teams (clinical operations, data science, biostatistics)
- Maintain complete and compliant study records per Azimuth SOPs and DoD requirements
- Perform protocol procedures as needed (e.g., phlebotomy, ECGs, specimen collection)
Required Qualifications
- Bachelor’s degree in science, public health, healthcare administration, or related field
- Minimum 5 years of clinical research experience
- Ability to obtain and maintain Secret Security Clearance (DoD requirement)
Highly Desired
- ACRP or SOCRA certification
- Experience in DoD, VA, or federal healthcare environments
- Strong knowledge of Good Clinical Practice (GCP)
- Experience with EHR systems such as MHS GENESIS (Cerner)
Why Join Azimuth Research Group?
If you thrive in a structured, compliance-driven research environment and are passionate about supporting impactful clinical studies within federal healthcare systems, we encourage you to apply.
#J-18808-Ljbffr”, “datePosted”: “2026-05-18”, “hiringOrganization”: { “@type”: “Organization”, “name”: “Azimuth Research Group”, “sameAs”: “https://uk.whatjobs.com/pub_api__cpl__435632220__4861?utm_campaign=publisher&utm_medium=api&utm_source=4861&geoID=8127” }, “jobLocation”: { “@type”: “Place”, “address”: { “@type”: “PostalAddress”, “addressLocality”: “Cornholme” } } }Azimuth Research Group is a life sciences research firm that leverages point-of-care data to address complex challenges for clients in the pharmaceutical, biotechnology, and academic sectors. Our vision is to transform the research landscape by embedding continuous, adaptive research into healthcare delivery ecosystems.
Location: Portsmouth, VA (Onsite)
Position Overview
Azimuth Research Group is seeking two full-time, on-site professionals to support clinical research operations within a Department of Defense (DoD) healthcare environment.
- Clinical Research Nurse (CRN)
- Clinical Research Coordinator (CRC)
Both roles play a critical part in executing clinical studies involving active-duty service members, veterans, and beneficiaries. These positions require strong clinical or research expertise, regulatory knowledge, and the ability to thrive in a structured, compliance-driven environment.
Clinical Research Nurse (CRN)
The Clinical Research Nurse combines direct patient care with protocol-driven clinical research execution. This role requires advanced clinical judgment, regulatory awareness, and strong collaboration across multidisciplinary teams.
Key Responsibilities
- Conduct clinical assessments, vital signs, and study procedures within scope of nursing practice
- Administer investigational products (as permitted) and monitor participants
- Support participant recruitment, screening, and informed consent
- Ensure compliance with GCP, FDA, ICH, and DoD Human Research Protection Program (HRPP) requirements
- Maintain accurate clinical documentation and support EDC query resolution
- Serve as a liaison between clinicians, research teams, and military personnel
- Support protocol adherence, deviation reporting, and audit readiness
- Collaborate with CRCs on regulatory documentation and study logistics
- Perform protocol procedures (e.g., phlebotomy, ECGs, specimen collection)
Required Qualifications
- Bachelor of Science in Nursing (BSN)
- Minimum 2 years of clinical nursing experience
- Ability to obtain and maintain Secret Security Clearance (DoD requirement)
- Strong clinical assessment and documentation skills
Highly Desired
- ACRP or SOCRA certification
- Knowledge of Good Clinical Practice (GCP)
- Experience with MHS GENESIS
- Experience in DoD, VA, or federal healthcare environments
Clinical Research Coordinator (CRC)
The Clinical Research Coordinator is responsible for the day-to-day coordination of clinical trials, ensuring operational excellence, regulatory compliance, and data integrity across study activities in a DoD healthcare setting.
Key Responsibilities
- Coordinate operational aspects of clinical research studies across assigned sites, including military treatment facilities
- Develop, maintain, and review regulatory documentation (e.g., ICFs, protocol amendments, IRB submissions)
- Support participant screening, eligibility verification, recruitment tracking, and scheduling
- Serve as a primary point of contact for site personnel, investigators, and DoD research offices
- Ensure compliance with GCP, FDA, ICH, and DoD HRPP requirements
- Perform data abstraction from Military Health Systems and ensure accurate entry into EDC systems
- Monitor protocol adherence and elevate deviations or safety concerns
- Support site visits, audits, and monitoring activities, including follow-up documentation
- Collaborate with cross-functional teams (clinical operations, data science, biostatistics)
- Maintain complete and compliant study records per Azimuth SOPs and DoD requirements
- Perform protocol procedures as needed (e.g., phlebotomy, ECGs, specimen collection)
Required Qualifications
- Bachelor’s degree in science, public health, healthcare administration, or related field
- Minimum 5 years of clinical research experience
- Ability to obtain and maintain Secret Security Clearance (DoD requirement)
Highly Desired
- ACRP or SOCRA certification
- Experience in DoD, VA, or federal healthcare environments
- Strong knowledge of Good Clinical Practice (GCP)
- Experience with EHR systems such as MHS GENESIS (Cerner)
Why Join Azimuth Research Group?
If you thrive in a structured, compliance-driven research environment and are passionate about supporting impactful clinical studies within federal healthcare systems, we encourage you to apply.
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