Clinical Research Coordinator B (Department of Obstetrics and Gynecology)

About the role

This position will assist in the management of research studies within the Division of UroGynecology. The incumbent will coordinate detailed chart review, data extraction and the collection of clinical data from health records, and assist in other smaller related projects such as consenting subjects, conducting participant visits, and organizing meetings. Responsibilities may also include assisting with Institutional Review Board (IRB) filings and inquiries, preparing manuscripts, grant proposals, and research-related presentations. The role involves close collaboration with the Principal Investigator, Director of Research Operations, and study team to identify problems, develop solutions, implement approved procedural changes, and monitor results. Additional responsibilities may include providing study coordination for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects.

Responsibilities

• Collect study data per protocol, including abstracting data from electronic health records and inputting data into electronic case report forms (CRFs) in dedicated electronic data capture (EDC) systems and/or study databases
• Coordinate regulatory paperwork, record and report adverse events, and prepare study documents such as protocols, operational manuals, consent forms, recruitment materials, and data collection forms
• Create and manage project-specific databases and surveys
• Comply with institutional policies, standard operating procedures (SOPs), and guidelines
• Consent participants and confirm eligibility in conjunction with investigators
• Oversee study activities of research assistants
• Act as a point person for the planning and implementation of studies
• Function with a greater level of independence and capacity than a Clinical Research Coordinator A
• Perform other duties as assigned

Position is contingent upon continued funding.

Qualifications

• Bachelor of Science degree and 2 to 3 years of experience or equivalent combination of education and experience required
• Strong written and verbal communication skills
• Familiarity with EPIC and REDCap preferred