Listed on Merck’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role oversees clinical trial operations for oncology drug development, managing investigator sites, recruitment, safety monitoring, and regulatory documentation. It suits experienced clinical research associates with oncology background who can coordinate between medical teams and company stakeholders.
Our summary, not Merck’s wording. The full posting is on their site.
Skills this role names
- Clinical Data Management
- Drug Development
- Microsoft Excel
- Microsoft Word
- PowerPoint
- Regulatory Compliance
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What they ask for
Required
- 4–5 years of oncology CRA experience
- Communication skills with physicians and clinical research coordinators
- Medical knowledge fundamentals
- Presentation ability to explain trial protocols and drug overviews
- Computer proficiency in Microsoft Office
- English proficiency (TOEIC 730+ for business email)
- Ability to work as part of internal project teams
- Ability to coordinate across global R&D departments
Nice to have
- Knowledge of GCP and internal SOPs
- Knowledge of the assigned trial drug and disease area
- English conversation ability for presentations and teleconferences
- Specialist knowledge in oncology