Research Coordinator - Clinical Trials Unit

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.
• Affix 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.
• Communicate directly with research collaborators, study sponsor, and study vendors.
• Manage research data in accordance with protocols established by sponsors and the Institute.
• Attend study and research related meetings, conferences, and teleconferences.
• Participate in research planning and development activities.
• 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.
• Affix and perform general administrative work, including: processing subject reimbursements and incentives, inventory and ordering supplies, and organizing service billing.
• Work closely with the Manager, Medical Program Operations to develop and implement standard operating procedures.

Qualifications

• Educational Requirement: Bachelor’s degree is required, preferably in psychology, mathematics/statistics, neuroscience, biology, biophysics, physics, chemistry, biochemistry, or another related field.
• Experience Requirement: Minimum two (2) years of research related work experience required.
• Pay Range: Minimum pay range USD $40,043.12/Yr., Maximum pay range USD $66,204.53/Yr.