EMEA Medical Communications Lead

Scholar Rock, Inc.; Zug; On-site; CHF 140,000 - 200,000; Full time

Job summary

Scholar Rock, Inc. seeks an Associate Director of Medical Communications, EMEA, to drive regional medical communications initiatives across Europe and align with global strategy.

Based in Europe, you will partner with EMEA Medical Affairs and local teams to adapt global materials for HCP audiences. In this role you will lead content localization, coordinate regional congress activities, and oversee vendors and timelines while ensuring regulatory compliance and scientific accuracy.

Qualifications

• Advanced scientific or healthcare degree (e.g., Pharm.D., Ph.D., or equivalent) preferred.
• 5+ years in Medical Affairs, medical communications, or related biopharma role; rare disease or neuromuscular experience preferred.
• Experience developing medical content for healthcare professional audiences and translating complex science into clear communications.

Responsibilities

• Execute regional medical communications activities aligned with Global Medical strategy with cross-functional teams.
• Develop and maintain global medical communications content for EMEA and country needs.
• Support congresses, symposia, abstracts, publications, and medical education initiatives.
• Localize and adapt materials for EMEA and country-specific needs with medical leads.
• Manage medical communications agencies, vendors, budgets, and timelines.

Skills

Medical communications

Project management

Scientific writing

Stakeholder management

Cross-functional collaboration

Education

Ph.D.

Pharm.D.

Master's degree in science

Job description

Scholar Rock, Inc. seeks an Associate Director of Medical Communications, EMEA, to drive regional medical communications initiatives across Europe and align with global strategy.

Based in Europe, you will partner with EMEA Medical Affairs and local teams to adapt global materials for HCP audiences. In this role you will lead content localization, coordinate regional congress activities, and oversee vendors and timelines while ensuring regulatory compliance and scientific accuracy.