Clinical Scientist, Oncology
About The Position
Corcept is leading the way in the research and development of cortisol modulators, molecules that regulate cortisol activity at the glucocorticoid receptor (GR). To date, we have discovered more than 1,000 selective proprietary cortisol modulators. In 2012, we received FDA approval of Korlym® (mifepristone), the first approved treatment for hypercortisolism (Cushing’s syndrome). Today, our team and collaborators continue to unlock the possibilities of cortisol modulation as a way to treat serious diseases. With more than 30 ongoing studies across a wide range of disease areas, including endocrinology, oncology, metabolism, and neurology, we remain dedicated to advancing the possibilities of cortisol modulation. What began as a ripple of scientific truth is now poised to unleash a sea change of discovery representing a fundamental shift in the way we understand and treat disease. The Clinical Scientist will ensure the clinical and scientific integrity of clinical trials conducted by Corcept in the Oncology therapeutic area.
Requirements
- 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
- Pharm D, PhD, MD or equivalent, preferably with experience in oncology therapeutic area(s)
- Applicants must be currently authorized to work in the United States on a full-time basis.
Nice To Haves
- 0-2+ years of relevant clinical development experience is preferred
- Relevant clinical research experience in academic settings is desirable
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
- Collaborate 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 clinical oversight and contributes to 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
- Serve as liaison to the commercial team on scientific issues
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Ph.D. or professional degree
