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Senior Medical Director Ophthalmology, Global Medical Affairs

Posted 27 Jun 2025
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Work experience
5 to 20 years
Full-time / part-time
Full-time
Job function
Degree level
Required language
English (Fluent)
Deadline
13 July 2025

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Senior Medical Director Ophthalmology, Global Medical Affairs

We are currently building a brand new Ophthalmology team, to carry out scientific work in the Retina space, with the aim to bring forward first in class products to address remaining unmet needs. We have an ambitious vision to create a world-class Medical Affairs organisation to help deliver these potential new therapies for patients.

We have an exciting, new role for a Senior Medical Director, Global Medical Affairs Ophthalmology.

You will be an individual contributor scientific leader and will be responsible for supporting the execution of scientific & medical affairs plans for your assigned Therapy Area (TA) in key countries and regions. You will be an impactful member of Product Development Team sub-teams and Global Human Health commercialisation teams. You will collaborate with our Early and Late Development R&D functional areas, Value & Implementation Outcomes Research (VIOR), Policy, Commercial and Market Access to address opportunities in key countries and engage with your network of scientific leaders and decision makers.

The primary location for the role will be London, UK, however, we are flexible for this role to be based in other key affiliates in Europe. You will be required to travel to various local markets as needed and retina congresses worldwide.

What you will do:

  • Support execution of the annual Value & Implementation plan with medical affairs colleagues from key countries and regions.
  • Serve as an impactful member of Product Development Team sub-teams (e.g., Clinical, V & I, Commercial, Publications).
  • Contribute to the development of a single global scientific communications platform.
  • Consolidate actionable medical insights from countries and regions.
  • Engage with a network of international scientific leaders and other key stakeholders (therapeutic guideline committees, payers, public groups, government officials, medical societies) about Our Company’s emerging science.
  • Organise global expert input events (advisory boards and expert input forums) to answer Our Company’s questions about how to develop and implement new medicines or vaccines.
  • Align plans and activities with Global Human Health (commercial) executive directors.
  • Organise global symposia and educational meetings.
  • Support key countries with the development of local data generation study concepts and protocols.
  • Review Investigator-Initiated Study proposals from key countries prior to headquarters submission (ex-USA).
  • Manage programs (patient support, educational or risk management) to support appropriate and safe utilisation of Our Company medicines or vaccines.

Qualifications, Experience, and Competencies:

Required:

  • M.D., Ph.D, or Pharm. D. in Ophthalmology, Optometry and recognised medical expertise within the pharmaceutical industry.
  • Experience in the Retina therapeutic space.
  • Experience in country/region medical affairs or clinical development.

Preferred:

  • Significant regional or global medical affairs experience (e.g., Regional Director Medical Affairs) with proven track record of contribution to medical affairs strategies.
  • Customer expertise, especially of scientific leadership and other key stakeholders (payers, public groups, government officials, medical professional organizations) in the assigned therapeutic area.

Skills/competencies:

  • Strong prioritisation and decision-making skills.
  • Ability to effectively collaborate with partners across divisions in a matrix environment.
  • Excellent interpersonal, analytical, communication skills (written and oral) in addition to results-oriented project management skills.

Your role at our company is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At our company, we’re inventing for life.

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively for the common good. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

Closing date for applications: 13th July 2025

About Us

We are one company, but we operate under two different corporate brand names. We are known as Merck & Co., Inc., Rahway, NJ, USA in the United States, Canada & Puerto Rico. We are known as MSD everywhere else.

MSD als werkgever
Keer op keer nieuwe uitdagingen aangaan, dat is wat bij je moet passen als je bij MSD aan de slag wilt. Want continu verbeteren is een van onze drijfveren. Dat geldt zowel voor werkprocessen als voor medewerkers. Gedrevenheid, teamwork en eigen initiatief zijn van groot belang. Bij MSD kun je je op allerlei manieren ontwikkelen. In de…


MSD als werkgever
Keer op keer nieuwe uitdagingen aangaan, dat is wat bij je moet passen als je bij MSD aan de slag wilt. Want continu verbeteren is een van onze drijfveren. Dat geldt zowel voor werkprocessen als voor medewerkers. Gedrevenheid, teamwork en eigen initiatief zijn van groot belang. Bij MSD kun je je op allerlei manieren ontwikkelen. In de diepte, door je te specialiseren in je vak. Maar ook door jezelf te verbreden en door te groeien naar een leidinggevende functie. Internationaal of juist heel lokaal, er zijn talloze andere mogelijkheden om stappen te zetten in je loopbaan, te rouleren in functies of te groeien in je functie. Werken bij MSD is werken in een dynamische high tech omgeving van internationale allure, die toch sterk lokaal geworteld is in Oss, Haarlem en Boxmeer.

Pharmaceutical
Haarlem
5,600 employees