Associate Director, Clinical Operations
Kymera Therapeutics · Watertown, MA
Clinical OperationsCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Associate Director of Clinical Operations at Kymera Therapeutics overseeing global clinical trial planning, execution, and oversight for targeted protein degradation therapies. The role involves managing study timelines, leading cross-functional teams, ensuring data integrity, and driving site engagement across immunological disease programs.
What they're looking for
- Bachelor's degree and 8+ years clinical operations experience
- Expertise in clinical trial design, protocol development, and regulatory documentation
- Strong project management and cross-functional team leadership skills
- Experience with site qualification, monitoring, and data management oversight
- Knowledge of clinical operations process improvement and quality standards
- Ability to manage vendor selection and CRO relationships
What you'll be doing
- Plan and execute global clinical trials from initiation through database lock
- Lead study meetings, investigator sessions, and training for internal and external teams
- Oversee site selection, qualification, and monitoring activities with quality oversight
- Manage study timelines, enrollment metrics, and protocol deviation tracking
- Collaborate with data management and translational medicine on data integrity and bioanalytical integration
Privacy & handoff
This role links to Kymera Therapeutics's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.