Overview:
The Research Coordinator in the Clinical Trials Unit assists and collaborates with the Principle Investigator (PI) and research collaborators to reach research goals. This position requires a degree of responsibility, flexibility, and independence to perform diverse duties including collecting, analyzing, and archiving data.
Responsibilities:
- Prepare and submit Institutional Review Board (IRB) required materials, as well as prepare compliance and regulatory documentation for local, state, and federal agencies and any other pertinent entity.
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Assist and perform duties under the direction of the Manager, Medical Program Operations. Support daily clinical trial and research study activities including: participant recruitment and scheduling, study procedure scheduling and coordination, obtaining results and ensuring clinician review, and documentation completion.
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Communicate directly with research collaborators, study sponsor, and study vendors.
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Manage research data in accordance with protocols established by sponsors and the Institute.
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Attend study and research related meetings, conferences, and teleconferences.
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Participate in research planning and development activities.
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Support data preparation, data entry, transfer, archiving, maintenance, and analysis as needed. Provide and communicate data-related study progress, issues, and problems to research collaborators.
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Assist with general administrative work, including: processing subject reimbursements and incentives, inventory and ordering supplies, and organizing service billing.
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Work closely with the Manager, Medical Program Operations to develop and implement standard operating procedures.
Qualifications:
Bachelor’s degree is required, preferably in psychology, mathematics/statistics, neuroscience, biology, biophysics, physics, chemistry, biochemistry, or another related field.
Minimum two (2) years of research related work experience required.