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
Preferred Skills, Qualifications and Technical Proficiencies:
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
Preferred Education and Experience:
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
Publications in peer-reviewed journals preferred
The pay range that the Company reasonably expects to pay for this headquarters-based position is $200,000- $269,800; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.
Applicants must be currently authorized to work in the United States on a full-time basis.
For information on how Corcept collects, uses, discloses, protects, and otherwise processes personal information and an explanation of the rights and choices available to you with respect to your personal information, please refer to our Privacy Notice link .
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.
Corcept will not conduct interviews via text message or messaging platforms and will not ask you to download anything as part of your interview. Though we use third-party tools to help with advertising our jobs, please be vigilant in checking that the communication is in fact coming from Corcept.
Benefits
Paid time off
Additional Information
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.
Corcepttherapeutics · Redwood City, CA