Leadership and local strategic planning and operational delivery of assigned clinical trials
Accountable for oversight of all assigned studies within the country
Planning and executing assigned country study goals and commitments
Develop and maintain optimal relationships with key institutions within the country
Drive the identification and inclusion of sites for diverse recruitment
Oversees regional study feasibility, site monitoring performance, quality metrics and all relevant activities
Collaborates cross-functionally to build and maintain strong relationships
Communicates regularly on country study status and escalates unresolved issues
Collaborates to develop and execute local implementation of risk management plans
Works with the Study Start-Up Team to ensure timely submissions and appropriate approvals
Maintains oversight and ensures consistency across studies and alignment across CROs

Minimum Bachelor’s degree
5-7 years of experience in Clinical Trial Operations in pharmaceutical / biotechnology industry or Clinical Research Organization, or equivalent
At least 3 years in a role of primary responsibility for clinical trial execution and management
Thorough understanding and experience in global clinical trials in a diverse range of patient populations
Preferred experience in both oncology and dermatology
Direct management experience and supervisory responsibility
Excellent interpersonal, organizational, problem-solving, and written/verbal communication skills
Proficient in Outlook/Word/Excel/PowerPoint
Must be able to travel (domestic and international) up to 10%.

Health benefits to include Medical, Dental and Vision
Company match 401k
Eligibility to participate in Employee Stock Purchase Plan
Eligibility to earn commissions/bonus based on company and individual performance
Flexible paid time off (PTO) and sick time

Associate Director, Clinical Trial Management

Key skills