Incyte Corporation is seeking a Senior Manager Clinical R&D QA to provide GCP oversight of clinical development programs. You will lead audits of investigator sites, vendors, and Trial Master Files, and coordinate inspection readiness and responses.
The role requires 5–7 years in GCP QA or clinical compliance, a science degree, excellent written and oral communication, and travel up to 30%. This office-based position is located in Wilmington, Delaware.
#J-18808-LjbffrSenior Manager, Clinical R&D QA – GCP Audits & Inspections in wilmington at Unknown Company
This position is listed as full time and onsite.