Associate Medical Director/Medical Director, Endocrinology and Metabolism

Corcept Therapeutics • Redwood City, CA

17h • $200,000 - $269,800 • Onsite

About The Position

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. 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.

Requirements

• MD or equivalent, board eligible or certified in internal medicine or internal medicine subspecialty preferred
• 2+ years’ clinical development experience in the biotechnology/pharmaceutical industry or an academic clinical trial unit
• Strong clinical and scientific knowledge
• Excellent communicator with proven leadership skills and the ability to interact in a cross functional environment
• Demonstrates agility to adjust workload based upon changing priorities
• Ability to drive timelines while maintaining quality and GCP compliance
• Applicants must be currently authorized to work in the United States on a full-time basis.

Nice To Haves

• Publications in peer-reviewed journals preferred

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 the clinical team
• Other duties as assigned

Benefits

• Corcept appreciates the commitment and hard work of all our team members as we strive to discover and develop novel treatments for patients with serious unmet medical needs.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level