Clinical Research Coordinator
About The Position
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.
Requirements
- Bachelor’s degree in related areas.
- 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.
- Tier1 NACI Investigation
Nice To Haves
- MS or MPH preferred.
- Minimum 2 years of experience as CRC preferred, preferably in DoD/military environment.
- Familiarity with eIRB system preferred.
Responsibilities
- 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.
- 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.
Benefits
- 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
- tuition reimbursement
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
101-250 employees
