Clinical Trial Docs & Records Lead (eTMF/CTMS) – Hybrid

A global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead. This role requires leadership in managing clinical documentation and records, ensuring compliance with regulatory standards, and overseeing clinical trial technologies. Candidates should have 8-10 years of experience in clinical operations and leadership skills, as well as familiarity with Veeva systems. A dynamic and supportive working environment is offered along with flexible working arrangements.