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Regulatory Affairs Manager
United States
Full Remote
AI Summary
Join our team as a Regulatory Affairs Manager to oversee all aspects of regulatory operations for Sarah Cannon site Clinical Operations. Develop and implement short- and long-term strategies for regulatory compliance. Work closely with department directors and industry sponsors.
Key Highlights
Regulatory Affairs Manager
Regulatory Operations
Clinical Trials
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Key Responsibilities
Manages, directs, plans and schedules activities and programs for the regulatory department
Establishes and enforces procedures that assure all trial teams and sites are fully compliant with all applicable laws, regulations, SOPs, and other applicable guidelines
Develops and implements regulatory policies and procedures for the sites and the site Clinical Operations team
Technical Skills Required
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Benefits & Perks
Comprehensive benefits
Total Rewards package
Competitive compensation package
Job Description
Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.
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