Clinical Research Manager III
California City, CA, United States On-site
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About the role
Accountable for all aspects of assigned clinical trials. Lead the Clinical Trial Team, who is responsible for planning, conducting and reporting of clinical trials. Author robust protocols with scientific rigor and quality. Trial conduct must be efficient, with seamless execution and timely reporting. Lead and matrix manage the global multidisciplinary Clinical Trial Team who is responsible for planning, conducting and reporting on all clinical trials within Development, including trials for Proof-of-Concept and Registration. Each Clinical Manager leads 2 or more clinical trial teams for studies of medium to high complexity in support of one or more projects. Contribute medical/scientific/feasibility input for the development of the protocol synopsis. Collaborate with the Medical Advisors to ensure country feedback is adequately integrated into the protocol. Independently ensure quality and timely execution of a clinical trial within timeline and budget Forecast trial resource needs. Accountable for the development, management and tracking of trial budget. Obtains approval for trial budget. Accountable for accuracy of trial information in all trial databases and tracking systems. Manages ongoing study budget.
What you'll bring
- University degree in Medical Science or equivalent education required.
- 9+ years in clinical research or relevant scientific, industry, therapeutic or geographic experience
- Relevant industry experience includes experience in planning and execution of clinical studies in various phases and geographies
- Solid understanding of the integrated development process of medical devices and/or pharmaceuticals
- Advanced degrees (e.g., MD, PhD, O.D., PharmD) are preferred.