Director, Science and Regulatory Policy Europe
Job Summary
Job Description
The Science and Regulatory Policy (SRP) team advocates for policy priorities that support the pipeline and portfolio for Research & Development and our companys business goals developing wider support for our causes and maintaining a strong reputation as a science-led biopharmaceutical innovative leader. We work in partnership with all of the R&D divisions to define and implement a prioritised policy and advocacy plan that advances business goals.
Our team is expanding hence we are recruiting for a Director Science and Regulatory Policy Europe to be based in Moorgate London as a primary location. Other locations in Europe such as Spain and Portugal will be considered.
- The successful candidate will perform the role from their respective country.
- Travel for this role is approximately 30% of the time.
- We operate on a hybrid working policy across our company locations.
The Science Regulatory Policy team comprises of four contributing teams:
- Global Regulatory Policy (SRP)
- Data & Advanced Digital Technology Policy (DADTP)
- Evidence Policy and
- Clinical Research Policy.
What you will do in this role:
- Develop and deliver strategic leadership for policy priorities to support our pipeline and portfolio
- Advocate for and anticipate policy change that affects our research and development activities worldwide and innovation environment
- Advise and provide insights for our research and development senior leadership on critical developments in the global policy environment that impact our pipeline and portfolio
- Take leadership for coordinating and aligning policy development and activity across research and development with focus on the Development and Regulatory organisations
- Leadership for strategy and coordination of R&D External Policy relationships to meet priorities
- Building our companys share of voice and influence extramurally to support the company enterprise policy agenda
You will:
- Shape and influence European science evidence and data/digital policy agendas to proactively enable R&D productivity scientific leadership and competitive pipeline advancement
- Drive early translation of emerging policy legislative and regulatory developments into decisionready insights risks and strategic options for pipeline portfolio evidence generation and access
- Set and advance company policy priorities on European science evidence data governance and advanced digital technologies ensuring alignment with R&D scientific strategy and enterprise innovation objectives
- Lead the development and execution of coordinated company policy positions and advocacy strategies on European legislative and regulatory initiatives mobilising crossfunctional alignment to shape outcomes
- Provide strategic leadership on European data and advanced digital technology policy including data integrity privacy security AI/ML digital health and cloudenabled collaboration to accelerate science and scale innovation
- Build and leverage strategic relationships with European and globally influential policymakers regulators research institutions and multilateral organisations to anticipate inflection points and influence policy direction
- Position the company as a scienceled industry leader by representing our company in external policy forums industry associations and professional settings
- Deliver forwardlooking policy analyses and executive briefings that inform senior R&D and company leadership on strategic choices tradeoffs and actions
What you need:
Required qualifications experience and skills:
- University Degree is required preferably in science health care public health or health policy; may be accompanied by a masters degree in science health care public health health policy or law
- Substantial experience in pharmaceutical biotech regulatory or science policy environments
- Proven experience in developing and articulating sciencebased policy positions white papers comment letters and briefing materials for senior leadership and external stakeholders
- Experience engaging in global science policy environments including US and European legislative regulatory and policy frameworks
- Experience advising senior leaders on science policy implications risk and strategic positioning
Preferred:
- Postgraduate degree in science policy health policy or law
- Skilled with AI Data and Real World Evidence.
- Broad understanding of pharmaceutical R&D including clinical development evidence generation or innovative development approaches
- Demonstrated leadership or active participation in industry trade associations scientific societies or multistakeholder policy initiatives
- Experience in working in the field of pharmaceutical/biotechnology development
Competencies/Skills
- Strong relationship management and interpersonal skills with superb written and oral and
- communication skills
- Strong interpersonal writing and communication skills with ability to demonstrate analytic thinking excellent presentation and negotiation skills
- Ability to thrive in a cross-functional team environment with a global mindset
- Excellent command of English (written and spoken)
- Data savvy with an eye for detail
Required Skills:
Adaptability Detail-Oriented Regulatory Experience Regulatory Law Regulatory Policies Regulatory Strategy Development Science Strategic Planning Strategic ThinkingPreferred Skills:
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Merck & Co. Inc. Rahway NJ USA also known as Merck Sharp & Dohme LLC Rahway NJ USA does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place introductions are position specific. Please no phone calls or emails.
Employee Status:
RegularRelocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
HybridShift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
08/10/2026*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Required Experience:
Director
About Company
Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more