
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 Senior Regional Clinical Research Associate (SRCRA) serves as the primary liaison to clinical trial sites participating in Corcept-sponsored studies. This role is responsible for managing site activities across all stages—qualification, initiation, monitoring, and close-out. The SRCRA ensures patient recruitment, enrollment, and overall site performance are aligned with GCP, ICH guidelines, and Corcept SOPs.
Site Monitoring & Oversight
Conduct qualification, initiation, interim, and close-out visits both remotely and on-site
Act as the main point of contact for site staff and ensure consistent communication throughout the study
Monitor site performance, including recruitment, enrollment, source data verification, protocol adherence, safety reporting, and data query resolution
Meet with the Principal Investigator during visits to discuss findings and next steps
Train site staff on protocol requirements, source documentation, and CRF completion
Prepare and submit visit reports and correspondence in accordance with the monitoring plan and SOPs
Regulatory and Documentation Compliance
Responsible for the collection and maintenance of regulatory documentation
Ensure accurate and timely IRB/EC submission, communication, and approvals are maintained within the Investigator Site File (ISF)
Reconcile ISF contents with Corcept’s eTMF to ensure completeness and accuracy
Responsible for conducting Investigational Product (IP) accountability and reconciliation, document destruction and return, and monitor re-supply and storage conditions
Ensure timely and appropriate SAE reporting and submission to IRBs
Site Communications & Relationship Management
Draft and deliver confirmation, follow-up, and monitoring visit reports (SQV, SIV, IMV, COV)
Maintain regular communication with the Lead RCRA (LRCRA) to report on site progress and resolve issues
Assess site readiness and resourcing (personnel, facilities, supplies) for trial conduct
Collaborate with vendors (e.g., central lab, imaging core) to resolve operational issues
Lead or participate in co-monitoring, oversight, and training visits as needed
Strong organizational and time management skills; capable of managing multiple priorities and deadlines
Excellent written and verbal communication skills; adept in regulatory and clinical terminology
Proven problem-solving and analytical skills
Leadership experience with the ability to mentor and train junior CRAs
Proficiency in Microsoft Word, Excel, and PowerPoint
In-depth knowledge of FDA regulations and industry practices
Willingness to travel up to 80% regionally, with occasional cross-country travel
Bachelor’s degree in science, healthcare, or nursing
6+ years of clinical trial experience, including at least 4 years as a regional field-based CRA
Familiarity with ICH-GCP guidelines and the ability to assess medical data
The pay range that the Company reasonably expects to pay for this position is $125,300 – $165,800; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.
#LI-Remote
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.
Please visit our website at: https://www.corcept.com/
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.
Originally posted by Corcept Therapeutics. View original posting
BioCareerAI is an independent job platform and is not affiliated with or endorsed by Corcept Therapeutics.
