Clinical Research Coordinator at SGS Australia Pty Ltd
New Jersey, New Jersey, USA -
Full Time


Start Date

Immediate

Expiry Date

20 Nov, 26

Salary

0.0

Posted On

22 Aug, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Yes

Skills

Industry

Biotechnology

Description

Clinical Research Coordinator (CRC) – Walter Reed National Military Medical Center


About Azimuth Research Group

Azimuth Research Group (Azimuth) is a global research organization that leverages point of care data to address challenging questions for clients in the pharmaceutical and biotechnology industry, as well as academia.


Our vision is to remake the biopharmaceutical and overall research industry by embedding continuous, adaptiveresearch into healthcare delivery ecosystems. We accelerate the discovery and development of therapies withintelligent precision--ultimately improving patient outcomes globally.


Location: Walter Reed National Military Center (WRNMC)


Position Overview

Azimuth Research Group is seeking a full-time, on-site Clinical Research Coordinator (CRC) to support clinical research operations within a Department of Defense (DoD) healthcare environment. This role supports clinical studies involving active-duty service members, veterans, and beneficiaries. The Clinical Research Coordinator will work closely with investigators, site personnel, and military research offices to ensure study compliance, participant safety, and data integrity.


Ideal Candidate

The ideal candidate will have prior experience supporting clinical research within military, federal, or highly regulated healthcare environments and possess a strong understanding of clinical trial operations, regulatory compliance, participant safety, and data management.


Key Responsibilities

  • Coordinate operational aspects of clinical research studies across assigned sites, including military treatment facilities.
  • Develop, maintain, and review regulatory documentation, including informed consent forms, protocol amendments, and 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 Human Research Protection Program (HRPP) requirements.
  • Perform data abstraction from Military Health Systems and ensure accurate entry into EDC systems.
  • Monitor protocol adherence and escalate deviations or safety concerns appropriately.
  • Prepare for and support site visits, audits, and monitoring activities, including follow-up documentation.
  • Collaborate with cross-functional teams including Clinical Operations, Data Science, and Biostatistics.
  • Maintain complete and compliant study records in accordance with Azimuth SOPs and DoD requirements.
  • Contribute to process improvement and quality initiatives across Azimuth’s research operations.
  • Attend study meetings, staff meetings, and investigator meetings as required.
  • Assist with regulatory submissions and ongoing regulatory maintenance activities.
  • Maintain flexibility to support study-related activities that may occur during early mornings, evenings, or occasional weekends.
  • Perform protocol procedures as needed, including phlebotomy, ECGs, and biological specimen collection.

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Responsibilities
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