Skip to main content

This job has expired

You will need to login before you can apply for a job.

Drug Safety & Pharmacovigilance Summer Intern

Employer
Corcept Therapeutics
Location
Menlo Park, CA
Start date
Jan 19, 2023

View more

Discipline
Administration, Clinical, Drug Safety/Pharmacovigilance
Required Education
Bachelors Degree
Position Type
Full time
Hotbed
Biotech Bay

Corcept is engaged in the discovery and development of drugs that treat severe endocrine, metabolic, oncologic and neurological disorders by modulating the effects of the hormone cortisol. Since 2012, we have marketed Korlym® for the treatment of patients suffering from Cushing’s syndrome, a life-threatening orphan disorder caused by excess cortisol activity.

In addition to our commercial product, Korlym, we have discovered a portfolio of more than 1,000 proprietary selective cortisol modulators.  Lead compounds are in Phase 2 and Phase 3 trials for the treatment of patients with Cushing’s syndrome, advanced ovarian cancer, castration-resistant prostate cancer, weight gain caused by antipsychotic medications and non-alcoholic steatohepatitis (“NASH”).  We are about to start a Phase 2 trial in patients with amyotrophic lateral sclerosis (“ALS”).

In 2021, we generated revenue of $366 million and net income of $112 million.

Come spend your summer working with passionate colleagues and inspirational leaders, all while gaining world-class experience in one of the fast-growing biotech in the Bay Area. 

 The Drug Safety and Pharmacovigilance (DSPV) organization works collaboratively and strategically with colleagues across the product lifecycle to identify, evaluate, understand, and communicate the safety profile of Corcept products to protect patients worldwide.

Responsibilities:

  • Supporting drug safety clinical trial start up and ongoing activities, including helping to establish safety management plans, setting up the serious adverse event (SAE) reporting processes, and SAE data reconciliation.
  • Performing quality review of adverse event (AE) reports processed and managed by third party vendors for both clinical trials and post marketed products.
  • Support effective monitoring of safety reports submissions to investigational sites, regulatory authorities, and ethics committees
  • Assist with generating reports from Safety database
  • Helping to collate and evaluate key performance indicators/metrics in support of the quality management system
  • Supporting department initiatives and projects, as assigned

Preferred Skills, Qualifications and Technical Proficiencies:

  • Knowledgeable in Microsoft Word, PowerPoint, and Excel preferred
  • Excellent verbal and written communication skills
  • Ability to work in teams and independently

Preferred Education and Experience:

  • Currently enrolled at an accredited university with a major in nursing, pharmacy, or other medical/health/life sciences major

The pay range that the Company reasonably expects to pay for this position is $19-29/hr; the pay ultimately offered may vary based on legitimate considerations, including job-related knowledge, skills, experience, and education.

Applicants must be currently authorized to work in the United States on a full-time basis.

If you are based in California, we encourage you to read this important information for California residents linked here.

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.

 Please visit our website at: https://www.corcept.com/

Corcept is an Equal Opportunity Employer

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert