Merck

This role supports global clinical trial operations within Merck's Human Health division, focusing on regulatory affairs. The intern will gain experience in clinical trial regulatory frameworks, Good Clinical Practices, and interactions with regulatory agencies. Key tasks include administrative support for regulatory submissions, monitoring dossiers, reviewing documents, coordinating information, editing informed consents, and participating in process improvement initiatives. The role requires a university degree in Pharmacy or Biochemistry and intermediate English skills.

Associate Specialist in Policy & Communications at Merck, supporting the implementation of internal and external communication plans. Responsibilities include content creation, managing communication channels, coordinating with external agencies, supporting corporate events, monitoring media, adapting regional campaigns, ensuring compliance with regulations, and providing administrative support. Requires a Bachelor's degree in Communications, Journalism, Public Relations, Marketing, or related fields, with 1-3 years of experience in corporate communications, PR, or marketing. Experience in regulated sectors is desirable. Strong writing, organizational, and interpersonal skills are essential.