LAVORO REGULATORY MEDICAL WRITING MANAGER PARMA, EMILIA ROMAGNA

Write and review the medical information content for global products under the direction of the medical information manager/lead... master in pharma medical affaires...

Air and care franchises are also supported by the medical affairs, value & access, and business excellence & customer experience global functions...

It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery...

Processes and tools     support the implementation and specific adaptation of procedures within rwe studies fulfil regulatory requirements and company strategic...

Be responsible for pharmacovigilance processes related to the assigned tools, including writing sops, wis, and internal guidelines... participate in audit and inspection...

Proven experience as clinical project manager... strong knowledge of clinical study design, clinical trial operations, gcp/ich guidelines and other applicable regulatory...