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The Translational Research Project Manager I, TRPM I, oversees the daily coordination and management of translational and biobanking research projects, which involves collecting various biological samples and clinical data. This role supports grant applications, progress reports, project initiation, regulatory compliance, and patient identification for research projects. The TRPM I bridges clinical and laboratory research by supporting both types of investigators. Additionally, the TRPM I indirectly supervises research coordinators and independently manages a portfolio of projects for each investigator. The specific tasks and responsibilities of the TRPM I vary based on departmental and investigator needs.
Job Responsibility:
Independent Project Management: Operate independently under the guidance of a senior manager, ensuring effective oversight and management of assigned projects
Grant Support: Assist the Principal Investigator (PI) with grant applications and progress reports
Regulatory Compliance: Support the PI in meeting regulatory requirements, including protocol submissions, amendments, and deviation filings
Collaborative Meetings: Lead and participate in meetings with internal and external collaborators
Staff Supervision Assistance: Assist Clinical Research Managers or Senior Translational Project Managers in supervising staff involved in project areas
Project Coordination: Responsible for the day-to-day coordination of research projects
Requirements:
Bachelor’s degree is required, Biology, biomedical sciences, public health, or related discipline
Three (3) years of experience in clinical research or project management, preference for experience in translational research projects
Experience with basic project management tasks, such as coordinating meetings and maintaining documentation
Experience in an academic institution with a proven track record of success in the clinical research field is preferred
Experience in knowledge of regulatory affairs, research ethics, and Responsible Conduct of Research (RCR) is preferred
Experience with basic grant writing and regulatory documentation is beneficial
Nice to have:
Experience in an academic institution with a proven track record of success in the clinical research field
Experience in knowledge of regulatory affairs, research ethics, and Responsible Conduct of Research (RCR)
Experience with basic grant writing and regulatory documentation