Associate Clinical Data Management Director
*Candidates need to work a hybrid model in Alameda, CA or King of Prussia, PA
Meet has partnered with a leading biotechnology company focused on developing innovative therapies for cancer, advancing a robust pipeline of small molecules and biologics through strategic partnerships and cutting-edge research. They are looking for an Associate Clinical Data Management Director to join their team and serve as the lead study data manager for a large, complex trial or multiple, smaller studies.
Key Responsibilities
- Work with different teams to plan and manage data tasks for clinical studies
- Make sure study documents are complete and data is accurate and ready on time
- Help design databases, check data quality, and support reports and submissions
- Guide team members, improve processes, and work with outside partners when needed
Key Qualifications
- Bachelor’s degree with 11+ years, Master’s with 9+ years, or PhD with 5+ years of related experience; at least 7 years in clinical data management and 4 years in a leadership role
- Strong experience with Electronic Data Capture (EDC); familiarity with IVRS/IWRS preferred
- Solid knowledge of GCP, FDA regulations, and CDASH/CDISC standards
- Proven skills in project management, problem solving, and effective communication
Please reach out to Martin Wenzel if you're interested in learning more: martin.wenzel@meetlifesciences.com