We are seeking a Clinical Research Supervisor (CRS) to join the Department of Psychiatry and Behavioral Sciences . In this role, you will work collaboratively as a member of our research team focused on responsibilities related to the day to day supervision of research teams and research operations. As a Clinical Research Supervisor, you will be an essential member of our team to ensure the proper oversight of clinical research protocols. As a CRS, you will supervise the day-to-day activities of Clinical Research Coordinators (CRCs), student affiliates and interns to ensure efficient and effective operations. You will be responsible for regulatory and data management activities and for data integrity associated with clinical research. Additionally, you will have the opportunity to participate in special projects and task forces as determined by management. We are looking for a dedicated, collaborative clinical research professional to take on this leadership role. This is an exciting opportunity to join a growing clinical research team. Apply today!

You will:

• Staff Management and Development - Participate in the orientation, training and supervision of CRCs; participate in facilitating departmental trainings; align staff and resources with appropriate protocols and research needs; and maintain workflow consistency among staff with standardized processes.
• Supervise and coordinate the day-to-day activities of CRCs to ensure efficient and effective operations of our research protocols.
• Operation Management - Ensure that workflow is managed and monitored to meet departmental and service needs; assist the Clinical Research Manager (CRM) with protocol activation, especially with start-up activities; monitor research portfolio for workload by appropriately managing and identifying service needs.
• Quality Assurance - Perform regular audits to ensure that the data collected is complete and accurate, and that the research project is carried out as planned.
• Regulatory Compliance - Ensure that all appropriate Institutional, State, and Federal regulations are followed throughout the course of a research project, database, or protocol. Also, you will ensure that research protocols are approved by the Institutional Review Board/Privacy Board (IRB/PB) and followed as written.
• Special Projects - Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. You will provide leadership, organizational, creative, or clerical support to established and new research initiatives.
• Lead and liaise meetings with a variety of stakeholders across multiples disciplines.
• Serve as key team member, providing support to direct report and clinicians on a daily basis.

You Have:

• At least 2 years of clinical research experience.
• Supervisory experience and experience with high volume trials is strongly preferred.
• Comprehensive knowledge and understanding of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA) is critical.
• Strong time management/project management skills.
• Knowledge of oncology-specific terminology is helpful.
• Experience with REDCap and/or building databases
• Knowledge of statistical software (SPSS, SAS or R) preferred
• Experience in the use of various electronic data management systems.

Hours:

Monday to Friday, 9 am to 5 pm.

Hybrid

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