Senior Manager, Clinical Quality Assurance

Corcept Therapeutics; Redwood City (CA); Hybrid; USD 173,000 - 204,000; Full time

Job summary

The Senior Manager of Clinical Quality Assurance (CQA) at Corcept Therapeutics leads day-to-day quality operations and compliance activities to support our clinical studies. This hybrid role requires on-site presence at least 3 days per week at our Redwood City headquarters.

The role focuses on GCP audits, risk-based oversight, inspection readiness, and collaboration with study teams to ensure regulatory compliance throughout the study lifecycle.

Qualifications

• BS/BA in science or related field or equivalent experience.
• 8+ years clinical research experience, 2+ years CQA experience preferred.
• Thorough understanding of Quality Systems that support GCP activities.
• Experience leading complex quality investigations, root cause analysis and CAPA.
• Experience developing GCP processes for best industry practices.

Responsibilities

• Develop/manage study audit plans ensuring compliance oversight for assigned studies by using a risk-based approach
• Lead/manage Good Clinical Practice (GCP) audits, including clinical investigator site, Trial Master File (TMF), and applicable study documents, including Clinical Study Reports (CSRs)
• Support clinical service provider and development internal process audits
• Assess changes to qualified service provider services and their impact to ongoing clinical studies
• Serve as a CQA Lead representative on assigned clinical studies and provide compliance support and oversight throughout the study lifecycle
• Support clinical study teams in risk management activities including the identification of critical to quality (CtQ) factors for each clinical study, implementing risk proportionate study activities in accordance with CtQs and the monitoring of identified risks to the CtQs
• Review clinical study documents and plans and provide CQA compliance review and approval of clinical development SOPs
• Manage and support GCP inspection readiness activities for assigned studies in alignment with study milestones
• Support clinical inspections conducted by regulatory agencies, including sponsor, clinical investigator site, and service provider inspections
• Lead critical investigations, to ensure regulatory reporting compliance
• Support, review and approve clinical non-compliance records (deviations and CAPA)
• Maintain a contemporary knowledge of agency and industry trends, standards, regulations and methodologies related to GCP
• Provide cross-training development opportunities to CQA team, and mentor/coach junior QA team members
• Some travel required

Skills

Quality Systems

GCP Audits

Audit Leadership

Risk Management

CtQ Risk Focus

SOP Review

Mentor/Coach

Education

BS/BA in science or related field

Job description

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 Manager of Clinical Quality Assurance (CQA) is a key member of the CQA team and will perform day-to-day clinical quality operations and compliance activities to support the success of the clinical studies sponsored by Corcept.

This is a hybrid role typically requiring on-site presence at least 3 days per week.

Responsibilities

• Develop/manage study audit plans ensuring compliance oversight for assigned studies by using a risk-based approach
• Lead/manage Good Clinical Practice (GCP) audits, including clinical investigator site, Trial Master File (TMF), and applicable study documents, including Clinical Study Reports (CSRs)
• Support clinical service provider and development internal process audits
• Assess changes to qualified service provider services and their impact to ongoing clinical studies
• Serve as a CQA Lead representative on assigned clinical studies and provide compliance support and oversight throughout the study lifecycle
• Support clinical study teams in risk management activities including the identification of critical to quality (CtQ) factors for each clinical study, implementing risk proportionate study activities in accordance with CtQs and the monitoring of identified risks to the CtQs
• Review clinical study documents and plans and provide CQA compliance review and approval of clinical development SOPs
• Manage and support GCP inspection readiness activities for assigned studies in alignment with study milestones
• Support clinical inspections conducted by regulatory agencies, including sponsor, clinical investigator site, and service provider inspections
• Lead critical investigations, to ensure regulatory reporting compliance
• Support, review and approve clinical non-compliance records (deviations and CAPA)
• Maintain a contemporary knowledge of agency and industry trends, standards, regulations and methodologies related to GCP
• Provide cross-training development opportunities to CQA team, and mentor/coach junior QA team members
• Some travel required

Preferred Skills, Qualifications and Technical Proficiencies

• Thorough understanding of Quality Systems that support GCP activities
• Experience developing GCP processes for the best industry practices
• Experience leading complex quality investigations, root cause analysis and corrective and preventative actions

Preferred Education and Experience

• BS/BA (science or related field) or equivalent experience
• 8+ years clinical research experience, 2+ years CQA experience preferred

The pay range that the Company reasonably expects to pay for this headquarters-based position is $173,430 – $204,030; 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.

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 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.