Tempus
Clinical Data Manager
Remote - Illinois · Manager · Full-time · Posted Sep 17, 2026
- Experience
- At least 8 years of related experience.
- Education
- BS/BA in a scientific discipline; MS or equivalent preferred.
About the job
Leads clinical data management activities for client studies throughout clinical drug development, from eCRF and database development through data review, database lock, and archiving.
What you'll do
- Lead and oversee clinical data management activities, including eCRF reviews, database build and testing, data cleaning, database lock, and archiving.
- Coordinate data review plans, data cuts and transfers, and collaboration with internal teams, CROs, and other vendors.
- Review study documentation, communicate data management plans and deliverables, and support GCP inspection readiness.
What they ask for
- At least 8 years of related experience in a CRO, pharmaceutical, biologics, or biotechnology company.
- Study/vendor oversight experience and experience with global studies using an outsourced CRO model.
- Expert knowledge of data management processes, EDC system design/build, and clinical trial/data management systems.
- Knowledge of ICH GCP, regulatory requirements including 21 CFR Part 11, and data standards such as CDISC SDTM and CDASH.
Nice to have
- Experience with Medidata Rave EDC, MedDRA, or WHODrug.
- Experience working for both a sponsor company and a CRO; early-phase clinical trial experience.
Tools
EDC, CDISC SDTM, CDASH, 21 CFR Part 11, Medidata Rave EDC, MedDRA, WHODrug, Microsoft Word and Excel
Model-written summary · the original posting is authoritative