Quality Lead, Clinical TMF & Audits

A biopharmaceutical company in Durham, North Carolina, is seeking an Associate / Manager, Quality to ensure compliant documentation and advance quality systems in clinical studies. Candidates should possess a Bachelor's in life sciences and 6-12 years of relevant experience, particularly in GCP Quality. Key responsibilities include managing TMF documentation, collaborating with teams, and supporting audit readiness. The ideal candidate will be detail-oriented with strong problem-solving and communication skills.

This role is a great opportunity for those driven by results.
#J-18808-Ljbffr