Clinical Research Manager

Merck Merck · Pharma · North Brabant, Netherlands

Clinical Research Manager at Merck responsible for designing, coordinating, monitoring, and reporting clinical studies for animal health vaccines. Requires a DVM or Master's in Life Sciences with 5-7 years of relevant experience and understanding of GCP.

What you'd actually do

  1. Lead the design, planning, and organization of clinical studies, including objectives, timelines, resources, budgets, and protocol development.
  2. Provide overall leadership, direction, and support to cross-functional study teams.
  3. Select and manage investigators, laboratories, CROs, and other external partners.
  4. Ensure timely submission and approval of study-related regulatory applications and licenses.
  5. Oversee study execution to ensure compliance with GCP, legal requirements, and internal policies.

Skills

Required

  • Clinical Research
  • Data Management
  • Ethical Standards
  • Project Leadership
  • Protocol Development
  • Scientific Writing
  • Stakeholder Relationship Management
  • Veterinary Research
  • Veterinary Vaccines

Nice to have

  • Good Clinical Practice (GCP)
  • Regulatory Approvals

What the JD emphasized

  • GCP Good Clinical Practices guidelines