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Clinical Trial Program Senior Manager
2 months ago
Position Overview:
We are seeking a highly skilled individual with extensive experience in human research studies, particularly in the realm of clinical trials. This role requires the ability to effectively train research personnel on the coordination and management of clinical trials.
Key Responsibilities:
This position is a leadership role within the Institute for Stroke and Cerebrovascular Disease. The successful candidate will possess a strong understanding of research compliance, have prior experience in conducting audits for clinical trial studies, and be adept at leading internal audits.
Experience with CAPA (Corrective and Preventative Action) plans is essential, as is the capability to supervise a team of 8 research staff in their daily activities.
Additional Duties:
The individual will be responsible for assisting in the development of research protocols and overseeing a program dedicated to peer-reviewed pilot studies.
This role will also involve managing and training staff on site development, the enrollment of human subjects, and the monitoring of clinical trials.
Study Management:
The focus will be on the management of multiple studies, with an expectation to familiarize oneself with the Standard Operating Procedures (SOPs) for each study.
Qualifications:
This is not a research administrator position (pre/post award); however, experience with grant applications, particularly for clinical trials, centers, and multi-component grants (e.g., program grants) is highly beneficial. Strong confidence, excellent presentation skills, and effective collaborative abilities are also required.