Corcept Therapeutics

Director, Medical Writing

Corcept Therapeutics · Redwood City, California, United States

Posted 20 days ago · $183,500 - $242,800

or apply directly on Corcept Therapeutics's site. We never take the application ourselves.

Is this posting real?

This role has been open
20 days
Corcept Therapeutics's roles stay open a median of 45 days
Reposted
No
Salary listed
Yes
91% of Corcept Therapeutics's roles list one
Ghost-job risk at Corcept Therapeutics
high
45 stale, 4 reposted of 88 open
Hiring momentum
110 roles opened in the last 90 days
↑ up vs. the prior 90 days
Last confirmed on the employer's board
2026-09-17

Measured from postings appearing on and disappearing from Corcept Therapeutics's own greenhouse board since 2026-08-03. Full hiring picture for Corcept Therapeutics.

About this role

The Director of Medical Writing at Corcept will lead medical writing efforts for regulatory documents related to clinical development programs. This role involves managing a team of medical writers, overseeing the creation of high-quality clinical documents, and ensuring compliance with regulatory requirements. The director will also mentor staff, refine writing processes, and maintain expertise in the company's investigational products and relevant guidelines.

Our read on this posting3.6out of 5
benefits
1/5
freshness
4/5
career value
4/5
role clarity
4/5
pay transparency
5/5

Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Corcept Therapeutics as an employer.

What you need

  • 10+ years of regulatory medical writing experience in the pharmaceutical industry
  • Experience managing a team
  • Ability to write and edit clinical study protocols, clinical study reports, and investigator’s brochures
  • Excellent writing skills and understanding of the drug development process
  • Proficiency in MS Office applications and electronic document management systems
  • BA/BS degree in a scientific field

Nice to have

  • Advanced scientific degree (PhD, PharmD, or MS)
  • Familiarity with US and European regulatory requirements
  • Successful track record in complex clinical/regulatory writing projects
  • Excellent attention to detail and multitasking abilities
  • Understanding of electronic Common Technical Document (e-CTD) requirements

Worth weighing

  • No specific benefits listed in the posting
  • Fast-paced small company environment may require adaptability
  • Pay range provided, but final offer may vary based on multiple factors

Summarised from Corcept Therapeutics's posting. Read the full original.

Listed by Corcept Therapeutics on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.

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