Clinical Research Coordinator

Bristol Bay Native Corportation • Fort Bragg, NC

8d • Onsite

About The Position

Glacier Support Services, LLC (GSS) is seeking a Clinical Research Coordinator on-site at Ft. Bragg, NC. Responsibilities: Support and conduct clinical research studies following the IRB approved research protocol. Interview patients 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 patient commitment and obtain informed consent following the approved research protocol. Interview patients for protocols and collect and analyze appropriate data for recruitment purposes. Educate patients on the research protocol and conduct all research activities in accordance with all applicable regulations and approved protocols. Schedule patient for appointments and visits and manage enrollment schedules for multiple studies. Prepares and maintains data and regulatory documents on patients following standard procedures and protocol.

Requirements

• Bachelor’s degree in related area.
• 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 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.
• Familiarity with eIRB system preferred.

Responsibilities

• Support and conduct clinical research studies following the IRB approved research protocol.
• Interview patients 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 patient commitment and obtain informed consent following the approved research protocol.
• Educate patients on the research protocol and conduct all research activities in accordance with all applicable regulations and approved protocols.
• Schedule patient for appointments and visits and manage enrollment schedules for multiple studies.
• Prepares and maintains data and regulatory documents on patients following standard procedures and protocol.

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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level