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