Corcept Therapeutics
Biotechnology/Pharmaceutical
AssociateMedicalDirector/MedicalDirector,EndocrinologyandMetabolism
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“Associate Medical Director/Medical Director, Endocrinology and Metabolism at Corcept Therapeutics. Skills: Clinical study design, Medical oversight, Data interpretation. Participate in design, development, execution of clinical studies. Participate in writing, review of clinical protocols”
Industry & Context.
Authorized to work in US
What They're Looking For.
Must Have
2+ years clinical development experience, MD or equivalent, Board eligible or certified in internal medicine or internal medicine subspecialty
Nice to Have
Publications in peer-reviewed journals
What You'll Do.
Participate in design
execution of clinical studies
Participate in writing
review of clinical protocols
Provide medical oversight for clinical trials
Monitor safety for clinical trials
Participate in safety committee
Analyze clinical data
Interpret clinical data
Present clinical data
Work with other development functions
Establish relationships with external experts
Serve as liaison to commercial team
Participate in regulatory discussions
Participate in regulatory activities
Provide disease area training
Provide scientific training
How You'll Work.
Team & Collaboration
Cross functional environment; Other development functions
Communication Scope
Excellent communicator
Full Job Description
For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com. The Associate Medical Director/Medical Director, will act as a key participant in the medical and scientific oversight of clinical studies in endocrinology and metabolism. Responsibilities: Participate in the design, development and execution of clinical studies across the development life cycle (Phase1-3) Participate in the writing and review of clinical protocols, investigator brochures, clinical study reports, and other documents Provide medical oversight and safety monitoring for clinical trials including review of AEs and SAEs, and participation in the safety committee Play a key role in the analysis, interpretation and presentation of clinical data Work closely and collaboratively with other development functions, e. g. clinical operations, safety, biometrics, regulatory, medical writing, to achieve project objectives Establish relationships with external experts in the relevant scientific areas, including principal investigators and opinion leaders, to facilitate scientific excellence in clinical trials research Serve as liaison to the commercial team on medical and scientific issues Participate in appropriate regulatory discussion and activities, including the filing of IND’s, CTXs, and NDA/MAAs Provide ongoing disease area and scientific training to members of t
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