Senior Medical Director, Neurology
- Employer
- Corcept Therapeutics
- Location
- Menlo Park, California
- Start date
- Dec 22, 2021
View more
- Discipline
- Clinical, Clinical Medicine, Clinical Project Management, Medical Affairs
- Required Education
- Doctorate/PHD/MD
- Position Type
- Full time
- Hotbed
- Biotech Bay
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Job Description
The Senior Medical Director will ensure the medical and scientific integrity of clinical trials conducted by Company in the therapeutic area of Neurology.
Responsibilities
- Act as clinical scientist and clinical subject matter expert for both Company team members and for external contacts related to the assigned therapeutic programs
Provide training and ongoing input to all members of the clinical team on medical and scientific issues related to the therapeutic field in question
Provide scientific oversight for Company operational staff, contract research organizations (CROs), and clinical trial sites in all areas related to the therapeutic programs
Design, develop and, implement clinical studies for the applicable drug candidate, from Phase I through Phase III
Develop and participate in the writing and review of protocols, investigator brochures, study reports and other clinical and regulatory documents
Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems and final reports
Acts to provide medical oversight and safety monitoring for ongoing clinical trials including participation in SAE reporting and serving on the safety committee
Play a key role in the analysis, interpretation and delivery of high quality clinical data
Interact with principal investigators and opinion leaders to facilitate clinical trials research
Participate in appropriate regulatory discussion and activities, including the filing of IND’s, CTXs, NDA/MAAs, throughout the development cycle
Participate in clinical study report conceptualization, development and writing for global regulatory submissions
Work closely and collaboratively with other functions, e.g. clinical operations, safety, biometrics, regulatory, medical writing, medical affairs and commercial
Develop and give internal and external presentations as subject matter expert for the therapeutic area
Participate in the development and review of publications
Prepare and monitor budgets in collaboration with clinical operations and R&D finance
Participate in the management of human resources in a matrixed environment – recruitment, performance management, succession planning, talent management, etc.
Serve as a liaison to the commercial team on medical issues
- MD, board certified (or eligible) preferably in Endocrinology
Requires at least 5 years of relevant clinical development experience
Relevant basic and/or clinical research experience in academic settings is viewed favorably
- Strong clinical and scientific knowledge
Excellent communicator with proven leadership skills and the ability to interact in a cross functional environment
Comfortable in a fast-paced and nimble small company environment and able to adjust workload based upon changing priorities
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