Job details

Associate Director, Process Development and Documentation, Clinical Quality Assurance

Corcept is dedicated to advancing the development of cortisol modulators for treating serious diseases. They seek an Associate Director to lead clinical quality assurance operations and documentation.

Skills

Technical writing
Process development
Regulatory compliance
Quality assurance
Team management

Responsibilities

Lead process development and documentation for clinical studies.
Manage cross-functional teams to develop GCP, GVP, and GLP SOPs.
Support clinical study teams with process compliance.
Participate in clinical study document reviews.
Lead quality management system improvements.
Oversee inspection readiness and preparation activities.

Education

BA/BS degree in biological sciences or related field

Benefits

Health insurance
Retirement plans
Paid time off
Professional development opportunities

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CEO of Corcept Therapeutics

Joseph K. Belanoff

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By Corcept Therapeutics

Corcept Therapeutics wants to help people who are beyond blue. The biotechnology firm is exploring treatments that regulate the presence of Cortisol, a steroid hormone associated with some psychiatric and metabolic disorders. It is developing its ...

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FUNDING

Public

DEPARTMENTS

Quality Assurance

SENIORITY LEVEL REQUIREMENT

Senior

TEAM SIZE

51-200

LOCATION