Scientific Affairs Manager — MC4R (UK & Ireland)

Rhythm Pharmaceuticals Inc.

England

Remote

GBP 90,000 - 130,000

Full time

14 days+

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Job summary

Rhythm Pharmaceuticals Inc. in the UK & Ireland is seeking a Scientific Affairs Manager to lead medical and scientific initiatives for rare MC4R pathway diseases, collaborating with national and international Medical Affairs to ensure compliance and scientific integrity.

You will build peer-to-peer relationships with KEEs and stakeholders, support research initiatives and advisory boards, and contribute to integrated tactical plans, while working with Drug Safety, Market Access and Commercial

Qualifications

  • Minimum 8 years in Medical Science Liaison or similar field.
  • Experience with MC4R pathway diseases is preferred.
  • Rare diseases launch experience is a plus.
  • Proven cross-functional collaboration across clinical, safety and commercial.

Responsibilities

  • Lead as SAM for UK and as a member of the international Medical Affairs team.
  • Be a subject‑matter expert for MC4R pathway diseases and indications.
  • Contribute to development and implementation of integrated strategic plans and tactics.
  • Organize and lead local advisory boards and Key External Expert meetings.
  • Provide medical support for local strategy implementation.
  • Collaborate with Drug Safety, Market Access, and Commercial teams.
  • Monitor Rhythm clinical trials taking place in the UK and follow up as needed.
  • Identify knowledge gaps and organize non-promotional scientific presentations.

Skills

Communication
Cross-Functional
Presentation skills
Strategic planning
Self-starter
UK healthcare
KOL engagement

Education

PharmD/PhD/MD

Job description

Rhythm Pharmaceuticals Inc. in the UK & Ireland is seeking a Scientific Affairs Manager to lead medical and scientific initiatives for rare MC4R pathway diseases, collaborating with national and international Medical Affairs to ensure compliance and scientific integrity.

You will build peer-to-peer relationships with KEEs and stakeholders, support research initiatives and advisory boards, and contribute to integrated tactical plans, while working with Drug Safety, Market Access and Commercial

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