What are the responsibilities and job description for the Manager, Clinical Quality Assurance position at Corcept Therapeutics?
The Manager of Clinical Quality Assurance position is an exciting opportunity to build upon solid clinical research experience to become a key member of the Clinical Quality Assurance team. This role will perform day-to-day clinical quality operations and compliance activities to support the success of the clinical studies sponsored or supported by Corcept. This is a hybrid role typically requiring on-site presence 3 days per week.
Responsibilities
- Lead/manage Good Clinical Practice (GCP) audits, including clinical investigative site audits, clinical vendor audits, clinical department internal audits, Trial Master File (TMF) audits, and applicable study document audits, including Clinical Study Reports (CSRs)
- Serve as a QA representative and support clinical study teams to provide compliance advice
- Participate in review and approval of clinical study documents and clinical SOPs / Guidance Documents
- Manage study-specific Clinical Study Audit Plans (CSAP) compliance for the assigned program by using a risk-based approach for Corcept clinical studies
- Review and approve investigational product (IP) temperature excursions to ensure release or rejection of IP on time
- Lead continuous improvement of the Clinical Quality Management Systems (CQMS) and processes, including creation and revision of SOPs for GCP compliance and excellence
- Manage and support inspection readiness activities for GCP
- Support clinical inspections conducted by regulatory agencies, including sponsor inspections, clinical investigative site inspections, and contract research organization (CRO) inspections
- Support GMP, GLP, and PV inspections
- Lead clinical non-compliance event investigations and CAPA implementation
- Perform quality metric analysis for clinical QA including study quality event trends from clinical process deviations / CAPAs to include a review of protocol deviations, safety, and other clinical data
- Maintain a contemporary knowledge of agency and industry trends, standards, and methodologies as related to GCPs. Maintain the GCP regulatory surveillance program
- Provide cross-training development opportunities to QA team members, and mentor/coach junior QA team members upon request or as an assigned supervisor
Preferred Education & Experience
- BA/BS degree in a relevant field, or equivalent experience
- 6 years’ clinical research experience
- Understanding of Quality Systems that support GCP quality activities
- Experience with advanced Microsoft Office applications (Word, Excel, PowerPoint)
- Experience developing GCP processes for the best industry practices and training
The pay range that the Company reasonably expects to pay for this headquarters-based position is $154,100 - $181,300; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.
Applicants must be currently authorized to work in the United States on a full-time basis.
Salary : $154,100 - $181,300
