Description
Kiniksa Pharmaceuticals is hiring an Associate Director, Clinical Data Management to lead data management across clinical studies from protocol review and study start-up through database lock, regulatory submission support, follow-up, and archival. The role oversees CRO data management, EDC and non-EDC data quality, database specifications, eCRF design, UAT, data transfers, audit readiness, and compliance with GCP, ICH, and FDA requirements. It is based in the Lexington, Massachusetts office and requires onsite work five days per week.
