Job Function
R&D Operations
Job Sub Function
Clinical Trial Project Management
Job Category
People Leader
All Job Posting Locations
Beerse, Antwerp, Belgium; Breda, Netherlands
Job Description
Johnson & Johnson is currently seeking a driven Senior Clinical Research Manager to join the growing Clinical Operations team in the Netherlands (Breda) and Belgium (Beerse). In this role, you will manage a team of Local Trial Managers, Site Managers, and Clinical Trial Assistants, focusing on trial delivery in oncology, site engagement, staff development, training/onboarding, and resource management. You are responsible for the successful execution of trials from country feasibility through study close‑out, ensuring quality and compliance with SOPs, HCC, and local regulations.
Principal Responsibilities
- People management: Provide line management, goal setting, performance evaluation and talent development; build, hire, and train a fully effective team; conduct site visits; forecast resource needs.
- Trial delivery & oversight: Accountable for feasibility processes, oversight of site selection, start‑up, execution and monitoring; ensure inspection readiness, adherence to ICH‑GCP, local legislation and SOPs; support audits, inspections and CAPA resolution.
- Continuous improvement & organizational change: Lead implementation of innovation, inspire change, cultivate learning, contribute to new process development, track metrics.
- Co‑develop country strategy and drive tactics to full implementation.
- Help shape the Dutch Clinical Trial Landscape.
- Participate in special (global) initiatives; may assume additional responsibilities such as 'Champion' or SME.
Education and Experience Requirements
- BA/BS degree in Life Sciences or related field (or 8‑10 years equivalent experience).
- Minimum 8 years of Clinical Research experience in pharmaceutical industry, CRO or investigational site.
- At least 2 years of line management experience (desirable).
- Proven leadership & communication skills, decision‑making, issue resolution.
- Strong interpersonal & influencing skills; engage with stakeholders.
- Flexible mindset; ability to collaborate and handle multiple priorities in a matrix environment.
- Solid understanding of GCP, local laws and regulations.
- Proficient in English and Dutch; French required for Belgium.
Required Skills
None listed.
Preferred Skills
- Budgeting
- Clinical Trial Designs
- Compliance Management
- Contract Management
- Developing Others
- Execution Focus
- Fact‑Based Decision Making
- Inclusive Leadership
- Laboratory Operations
- Leadership
- Process Improvements
- Productivity Planning
- Project Integration Management
- Research and Development
- Research Ethics
- Resource Planning
- Team Management