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Posted 1mo ago

Clinical Research Coordinator

@ Bristol Bay Native Corporation
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Fort Bragg, North Carolina, United States
OnsiteFull Time
Responsibilities:support studies, interview participants, collect data
Requirements Summary:Bachelor’s degree; MS or MPH preferred. 2+ years CRC experience preferred, especially in DoD/military settings. Knowledge of human subject protections and regulatory compliance.
Technical Tools Mentioned:Microsoft Office, eIRB, IRB systems, Data management
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Job Description

We are Glacier Support Services (GSS), LLC, a government contracting and consulting firm supporting several military installations and federal agencies across the nation. GSS is seeking a Clinical Research Coordinator on-site at Ft. Bragg, NC.

 

What You'll Do:

  • Support and conduct clinical research studies following the IRB approved research protocol.
  • Interview potential participants for protocols and collect and analyze appropriate data for recruitment purposes.
  • Review new patient records and screen patients for eligibility to participate in the research protocol.
  • Determine participant commitment and obtain informed consent following the approved research protocol.
  • Interview participants for protocols and collect and analyze appropriate data for recruitment purposes.
  • Educate participants on the research protocol and conduct all research activities in accordance with all applicable regulations and approved protocols.
  • Schedule research participants for research appointments and related visits and manage enrollment schedules for multiple studies.
  • Prepare and maintain data and regulatory documents on participants following standard procedures and protocols for multiple studies.

What You Bring:

  • Bachelor’s degree in related areas.  MS or MPH preferred. 
  • Minimum 2 years of experience as CRC preferred, preferably in DoD/military environment.
  • Strong knowledge of research regulations, especially relating to protection of human subjects and clinical data. 
  • Demonstrated ability to work both collaboratively and independently.  Collegiality in team environment.  Excellent judgment.
  • Good problem-solving skills with proven ability to strategize, prioritize and multitask to meet goals/deadlines. 
  • Competent in Microsoft Office (Outlook, Word, Excel, Teams, and PowerPoint). 
  • Excellent computer skills and attention to detail required. Familiarity with eIRB system preferred.
  • Experience writing and submitting protocols, modifications, continuing review reports, and other necessary reports to IRB.
  • Experience conducting quality assurance procedures for protocol regulatory documents and maintenance of all regulatory documents and files.
     

Requirements: Tier1 NACI Investigation

GSS offers a competitive benefits package to include: paid holidays, paid time off including sick and vacation leave, medical, dental and vision insurance, flexible spending accounts, short and long term disability, company paid life insurance, 401(k) with a company match and discretionary profit sharing and tuition reimbursement.