msd

Clinical Research Associate

Apply Now

At a Glance

Location
NLD - North Brabant - Boxmeer, Netherlands
Work Regime
hybrid
Employment
Full time
Posted
2026-06-23

Key Requirements

Required Skills

Data AnalysisGCPMicrosoft Office

Domain Knowledge

  • Clinical
  • Regulatory

Benefits & Perks

Time Off

allowance; 35,5 days of leave; Attractive collective health

Requirements

Proven experience in a clinical research role, preferably in animal health or related field.

Strong understanding of Good Clinical Practice (GCP) and clinical study processes.

Experience with Electronic Data Capture (EDC) systems preferred.

Clinical Research, Data Analysis, Good Clinical Data Management Practice (GCDMP), Good Clinical Practice (GCP), Interpersonal Relationships, Project Management, Regulatory Compliance, Regulatory Requirements, Veterinary Medicine

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.

Compensation & Benefits

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.

Competitive salary and a 3% year-end allowance;

35,5 days of leave;

Attractive collective health care insurance package with considerable reduction rates;

Solid Pension Plan;

Annual bonus based on own and company performance;

Responsibilities

As a Clinical Research Associate, you will independently manage and monitor clinical study activities at site level.

You will ensure that clinical studies are conducted in compliance with study protocols, Good Clinical Practice (GCP), VICH guidelines and applicable regulatory requirements.

You will collaborate closely with the Clinical Study Team, Data Management and external partners to ensure accurate data collection, proper documentation and timely execution of study activities.

Conduct site visits (initiation, interim, and close-out) across CROs, veterinary clinics and farms, ensuring study compliance.

Prepare, maintain and review study documentation, including study files and CRFs, in collaboration with the study team.

Support site selection and assist in engaging investigators, laboratories and external partners.

Team

Our Clinical Research team is responsible for the execution and monitoring of clinical field studies across Europe that support the development of animal health products. We work closely with internal and external stakeholders including Contract Research Organizations (CROs), veterinary clinics, farms, and laboratories to ensure high-quality data and compliance with regulatory standards. The team is part of the global Research & Development organization, contributing to innovative solutions for animal health.

About the Company

Please send an email including the vacancy number and job title to the following email address:

RecruitmentNL@MSD.com

.