Clinical Operations Compliance Director

Providing strategic leadership in compliance, the full-time Clinical Operations Compliance Director will ensure oncology clinical research activities adhere to regulations and industry standards while managing risk, issue oversight, and inspection readiness in a remote environment. Key responsibilities Lead the execution and improvement of the Clinical Operations risk and issue management program Collaborate with Clinical Operations and cross-functional teams to assess and mitigate risks impacting clinical trial quality and compliance Drive consistency in clinical trial execution through the development and implementation of standardized processes and best practices Required qualifications Bachelor's degree in a related discipline with a minimum of 13 years of experience, or a Master's degree with 11 years, or a Doctoral degree with 8 years of experience Experience in the biotech or pharmaceutical industry, including roles with CROs and R&D outsourcing Demonstrated leadership and management skills in a relevant industry role In-depth knowledge of biopharmaceutical industry regulations and best practices Strong analytical and strategic thinking skills with the ability to adapt in a fast-paced environment