LAVORO REGULATORY MEDICAL WRITING MANAGER PARMA, EMILIA ROMAGNA

Master in pharma medical affaires will be a plus... write and review the medical information content for global products under the direction of the medical information...

Education master’s degree in science, phd or similar preferred languages english fluent technical skills capacity to work on situations or data requiring an in-depth...

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

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

Languages fluency in english (both spoken and written)   technical skills well-rounded knowledge of pharmaceutical drug development, regulatory and ip framework...

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