Job Summary
The Associate Director is tasked with overseeing clinical data collection standards and managing the programming activities within Medidata Rave. This role involves supervising study builds and evaluating the performance of external vendors, ensuring that all aspects of data integrity and study timelines are met through effective collaboration with various cross-functional teams.
Responsibilities
- Oversee the management of clinical data collection standards.
- Supervise Medidata Rave programming and study builds.
- Assess and ensure the performance of external vendors.
- Maintain the Rave Global Library to ensure data accuracy.
- Collaborate with cross-functional teams to meet project deadlines.
Qualifications
- A bachelor’s degree with a minimum of 10 years of related experience, or a master’s degree with at least 8 years of experience.
- Proven, extensive hands-on experience with Medidata Rave programming.
- Experience in configuring clinical study databases.
- Solid understanding of CDISC standards.
Revolution Medicines provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
