Ensure study completion within timelines and budget
The Associate Director, Clinical Study Management, will be responsible for overseeing the execution of clinical trials in oncology and other therapeutic areas, as required
Job Summary
The Associate Director, Clinical Study Management, will be responsible for overseeing the execution of clinical trials in oncology and other therapeutic areas, as required.
This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our California or New Jersey offices.
Responsible for hiring, performance management, career development, and providing mentorship to Clinical Study Management personnel.
Matching Summary
The Associate Director, Clinical Study Management, will be responsible for overseeing the execution of clinical trials in oncology and other therapeutic areas, as required.
Skills & Requirements
Must-have
Oversee clinical trial execution
Oncology and other therapeutic areas
Ensure study completion within timelines and budget
Global clinical operational experience
ICH-GCP, EMA, PMDA regulations
Nice-to-have
Passion for excellence in advancing patient care
Solutions oriented and flexible
Key Requirements
Minimum of 10 years of related experience with a Bachelor’s degree or 8 years and a post-graduate degree
Experience leading large, global clinical trials
In-depth knowledge of ICH-GCP, EMA guidelines
Proven ability to manage clinical studies within timelines and budgets