Job Description
Be part of a collaborative and forward-thinking environment that is shaping the future of animal health through cutting-edge vaccine development and impactful clinical studies. Join us a a:
Clinical Research Manager
Welcome in our team
Our Clinical Research team in Boxmeer is responsible for the execution of clinical studies in Europe related to the (further) development of vaccines for animal health. The team plays a key role in creating clinical and scientific evidence for mainly our animal health biological development projects executed in Boxmeer. The team is part of the Research & Development organization, which develops pharmaceutical and biological animal health products for the global market. Within our Biological R&D department in Boxmeer, we employ leading scientists who undertake cutting edge research using a broad array of novel technologies.
About the role
As a Clinical Research Manager you will act primarily as the Clinical Study Team Leader and you will be responsible for designing, coordinating, monitoring and reporting assigned and project based clinical field studies that will support the regulatory approval of new and existing companion animal and livestock biologicals. You ensure these studies are conducted in compliance with the requirements of Good Clinical Practice (GCP) and within agreed budget and timelines. This role requires close collaboration with internal (Research & Development, Regulatory Affairs) and external (Contract Research Organizations (CROs), Veterinarians, Farmers, Universities) stakeholders.
Tasks and responsibilities include but are not limited to:
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Lead the design, planning, and organization of clinical studies, including objectives, timelines, resources, budgets, and protocol development.
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Provide overall leadership, direction, and support to cross-functional study teams.
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Select and manage investigators, laboratories, CROs, and other external partners.
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Ensure timely submission and approval of study-related regulatory applications and licenses.
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Oversee study execution to ensure compliance with GCP, legal requirements, and internal policies.
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Plan and coordinate monitoring, data management, and clinical supply activities.
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Maintain effective communication with all stakeholders and provide regular updates on study progress.
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Prepare, review, and finalize study documentation, including protocols and final study reports.
Your profile
- Doctor of Veterinary Medicine or a Master’s degree in Life Sciences.
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At least 5-7 years combining relevant experience in a (biotechnical) company with relevant veterinary or agricultural experience.
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Experience in a clinical study related role.
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Understanding of GCP Good Clinical Practices guidelines.
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Able to extract the essence of scientific data and translate these into well-written documents.
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Willing to occasionally travel within Europe.
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Excellent command of English; Dutch is a plus.
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Living at a reasonable distance from Boxmeer.
What we offer
We welcome you to a truly global, dynamic and challenging environment with great opportunities for personal development. Our benefits are very competitive, and the summary below will give you an idea of what you can expect.
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Competitive salary and a 3% year-end allowance;
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35,5 days of leave;
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Attractive collective health care insurance package with considerable reduction rates;
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Solid Pension Plan;
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Annual bonus based on own and company performance;
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Travel allowance for commuting;
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A high‑quality company restaurant offering fresh and healthy options every day.
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Excellent accessibility: the train station is located directly next to our main entrance, and there is ample parking available.
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A contribution toward your personal sports membership to support your vitality.
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A beautiful private park on site - perfect for a walk, a break or a moment of relaxation.
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Mental well‑being support through Lyra Health for you and your family members.
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Access to a dedicated prayer/meditation room.
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Extensive growth opportunities thanks to the size of the site and the wide range of disciplines and global departments represented in Boxmeer.
Animal Health
Our Animal Health Division is a trusted global leader in veterinary medicine, dedicated to preserving and improving health, well-being, and performance of animals and the people who care for them. We are a global team of professionals working together to make a positive difference in animal care and the world’s food supply and have a deep sense of responsibility towards our customers, consumers, animals, society, and our planet.
Through our commitment to The Science of Healthier Animals®, we offer veterinarians, farmers, pet owners and governments one of the widest ranges of veterinary pharmaceuticals, vaccines and health management solutions and services as well as an extensive suite of digitally connected identification, traceability and monitoring products. We invest in dynamic and comprehensive R&D resources and a modern, global supply chain. We are present in more than 50 countries, while our products are available in some 150 markets.
For questions about this vacancy
Please send an email including the vacancy number and job title to the following email address: [email protected].
Required Skills:
Clinical Research, Data Management, Ethical Standards, Project Leadership, Protocol Development, Scientific Writing, Stakeholder Relationship Management, Veterinary Research, Veterinary Vaccines
Preferred Skills:
Good Clinical Practice (GCP), Regulatory Approvals
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
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:
Regular
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Hybrid
Shift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
06/16/2026
- A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID:R399604
