This is a legal internship position within Merck's Clinical Research department, focusing on supporting the financial and administrative aspects of clinical trials. The role involves assisting with budget negotiation, contract drafting, patient payment management, and documentation archiving. It is a 12-month internship, with a possibility of extension, and requires a background in legal studies and a Master's in Clinical Research or similar.

This role is responsible for ensuring the scientific, ethical, and regulatory integrity of all medical-scientific information activities within the company, in full compliance with AIFA regulations, the Farmindustria Code of Ethics, and internal policies. It oversees medical review activities for promotional and external materials, disease awareness campaigns, and other product- or therapy area-related communications, while also serving as the accountable leader for the local Designated Point of Contact for medical, safety, and product quality inquiries. In addition, this role leads and develops a team by fostering a collaborative, inclusive, and high-performing environment grounded in constructive feedback, effective delegation, and strong interpersonal awareness.