Associate Director, Clinical Data Management
Hybrid Role - 2-3x per week in Alameda, CA
Meet has partnered with a well-established oncology company that is looking to expand their Clinical Data Management team. They are looking for an Associate Director of CDM to join their team and support their ongoing P3 studies.
Key Responsibilities
- Lead CDM activities across complex clinical trials or programs from start-up through regulatory submission, ensuring quality and compliance.
- Collaborate cross-functionally with internal teams and external partners to manage timelines, resolve data issues, and drive study deliverables.
- Oversee vendors and team members, providing direction, training, and mentorship while ensuring accountability across studies.
- Drive process improvements within CDM, contributing to SOP development, innovation initiatives, and data quality standards.
Key Qualifications
- 8+ years of industry CDM experience
- Phase III experience required, NDA/BLA experience preferred
- Oncology experience required
- Ability to work a hybrid schedule