Regulatory Jobs
Hero Gradient Background
Corcept Therapeutics logo

New · posted Oct 31

Corcept Therapeutics · Pharmaceuticals

Clinical Research Associate II

  • Redwood City, CA
  • On-site
  • Full-time
  • Associate & Specialist
Save
EmploymentFull-time
DeadlineOpen until filled

The role

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 Clinical Research Associate (CRA) II monitors clinical study activities to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), and study protocols. This is an onsite role.

What you need

Preferred Education & Experiencenice to have

  • BS / BA (science or health care field) or RN
  • 3+ years’ experience as a CRA or field monitor at least some of which was in a big pharma or big CRO setting
  • Additional experience in the pharmaceutical industry is desirable

Preferred Skills & Experiencenice to have

  • Knowledge of the clinical trials process, the application of SOPs, and medical terminology
  • Therapeutic and protocol knowledge
  • Excellent verbal and written communication skills
  • Knowledge of GCP regulatory requirements
  • Knowledge of drug product supply requirements
  • Ability to handle multiple tasks with competing priorities
  • Ability to utilize a wide range of computer applications and tools

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

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 you'll do

  • Supervises study preparation, site preparation and the in clinic phases directly or through a CRO for assigned studies
  • Ensures that GCPs and Corcept clinical SOPs are met throughout the clinical program
  • Acts as liaison with clinical vendors and other functional area team members to meet project goals
  • Coordinates cross-functional components of the clinical trials process such as drug product supplies, etc.
  • Participates in the preparation and negotiation of clinical trial agreements and study budgets
  • Produces RFPs and participates in the evaluation and negotiation of bids from prospective vendors
  • Shares protocol writing with the medical director and biostatistician and ensures that all boilerplate requirements are met
  • Drafts informed consent forms ensuring that they are in agreement with the protocols
  • Participates in the development of study related documents including CRFs, study manuals and related documents
  • Coordinates all study start up activities, potentially with and through the CRO
  • Participates in site management and monitors study sites in the field with the CRO or independently on an as needed basis
  • Collects, reviews and tracks essential trial documents
  • Provides the clinical team and the program team with information regarding CRO and clinical site performance and recommend remediation when needed
  • Participates in study management to ensure study project goals are met
  • Other duties as assigned

Pay

$129,400 – $152,300 a year

Employer provided
How this compares

The pay range that the Company reasonably expects to pay for this headquarters-based position is $129,400 – $152,300; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

Where you'll work

Redwood City, CAOn-siteOpen in Maps (opens in a new tab)

More jobs in Redwood City, CA
Equal opportunity, accessibility and legal noticesCorcept Therapeutics's statements, word for word

Corcept is an Equal Opportunity Employer

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.

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.

Job intelligence

The context around this role

Live data · October 31, 2026

Salary intelligence

How the pay compares

This role's midpoint is 22% above the US median for Clinical Research roles at this level.

This roleEmployer provided

$129,400 to $152,300 a year

Associate & Specialist roles in the US7 roles publishing pay

Middle half $110,000 to $123,500, median $115,000
Annual base pay
Annual base payLowMedianHigh
This role$129,400—$152,300
All US$110,000$115,000$123,500

This role: Corcept Therapeutics's own published range. Comparisons: the base pay employers published on open Clinical Research roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Research

The general path across 14 open Clinical Research roles on Regulatory Jobs, with the titles they carry most. Not Corcept Therapeutics's own promotion track.

  1. This role

    Associate & Specialist

    Often: Clinical Research Associate

    $115K median7 open
  2. Next step

    Senior & Principal

    Often: Senior Clinical Research Associate · Clinical Research Associate

  3. Later

    Director

    Often: Associate Director, Site Monitoring · Director, Clinical Trial Liaison

Skills DNA

What this role leans on

How many of the posting's 31 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 2 linesDocumentation and SOPs: 6 linesData and digital systems: 1 lineClinical trial conduct: 13 linesCollaboration and leadership: 5 linesGMPDocumentationData systemsClinical trialsTeamwork
  • Clinical trial conduct13
  • Documentation and SOPs6
  • Collaboration and leadership5
  • GMP and compliance2
  • Data and digital systems1

Regulatory intelligence

The rules behind this role

Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

Company hiring pulse

Corcept Therapeutics on Regulatory Jobs

22
Open roles
22
Distinct roles
1
Locations

By discipline

  • Clinical17 77%
  • Regulatory3 14%
  • Quality2 9%

By level

  • Director10 45%
  • Senior & Principal5 23%
  • Manager4 18%
See all 22 Corcept Therapeutics roles

More roles at Corcept Therapeutics

All 22 Corcept Therapeutics roles

Similar Clinical Research roles elsewhere

Clinical Research Associate II at Corcept Therapeutics

Open until filled. $129K–$152K a year, employer provided.

Job alerts