Associate Director, Clinical Operations
kymeratherapeutics · Watertown, MA
- Posted
- 3 days ago
- Last confirmed live
- 2 days ago
What this role involves
This role oversees global clinical trials, manages study timelines and vendors, ensures data integrity and compliance, and leads site engagement and oversight activities.
Skills this posting asks for
- clinical trial management
- ich-gcp
- regulatory compliance
- site management
- vendor management
- data management
- monitoring
- informed consent
- ecrf design
- study start-up
- feasibility
- protocol deviation management
- outsourcing
- rfp
- sponsor oversight
- kpi/kri
- risk management
- training
- team leadership
Requirements
- 8 years of experience
- Level: director
From the employer’s posting
Who we are: Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to…
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