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Senior Manager Clinical Operations

Job in 4800, Breda, North Brabant, Netherlands
Listing for: Johnson & Johnson
Full Time position
Listed on 2026-06-13
Job specializations:
  • Management
    Operations Manager, Program / Project Manager, Healthcare Management
Salary/Wage Range or Industry Benchmark: 40000 - 60000 EUR Yearly EUR 40000.00 60000.00 YEAR
Job Description & How to Apply Below

Johnson & Johnson is seeking a driven Senior Clinical Research Manager to join our 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. The Senior Clinical Research Manager is responsible for the successful execution of trials from country feasibility through study close-out while maintaining oversight of quality & performance indicators, timelines, and compliance with SOPs, HCC, and local regulatory requirements.

Principal

Responsibilities:
  • People management: Provide line management to your team including goal setting, performance evaluation, and talent development; build, hire, and train a fully effective team; conduct accompanied site visits; evaluate and forecast resource needs and manage your team's workload.
  • Trial delivery & oversight: Accountable for robust feasibility processes and oversight of site selection; responsible for start-up, execution, and monitoring of trials in assigned therapeutic area(s); empower your team to deliver and think out of the box; ensure inspection readiness at all times, adherence to ICH‑GCP, local legislation and relevant SOPs; support your team in site engagement, issue resolution, and stakeholder management;

    support audits, inspections and timely CAPA resolution; build and shape internal and external network in assigned therapeutic area.
  • Continuous improvement & organizational change: Lead implementation of innovation and inspire change in the local organization; cultivate an environment that encourages shared learning, out of the box thinking and a "Yes we can!" mentality; contribute to the development of new processes or improvement initiatives; keep close oversight of metrics and drive follow‑up actions proactively.
  • Co‑develop country strategy and drive tactics to full implementation.
  • Help shape the Dutch Clinical Trial Landscape.
  • Participate in special (global) initiatives as assigned. May assume additional responsibilities or special initiatives such as "Champion" or "Subject Matter Expert".
Education and Experience Requirements:
  • BA/BS degree in Life Sciences or related scientific field (or 8‑10 years equivalent experience) with a minimum of 8 years of Clinical Research experience in pharmaceutical industry, CRO or investigational site. Other relevant working experiences and skills may be considered by the hiring manager.
  • At least 2 years of line management experience desirable.
  • Proven leadership & communication skills – ability to champion team productivity and cohesiveness.
  • Solid decision‑making and effective issue resolution skills; ability to generate & implement contingency plans for productivity & quality issues.
  • Strong interpersonal & influencing skills; willingness to engage with internal and external stakeholders (key sites, trade association, authorities and ethics committees).
  • Flexible mindset and ability to work in a constantly evolving environment with the ability to collaborate and handle multiple priorities in a matrix environment.
  • Strong proven understanding of GCP, local laws, and regulations.
  • Proficient in English and Dutch; for candidates based in Belgium, proficiency in French is also required.
Required Skills:
  • Budgeting
  • Clinical Trial Designs
  • Clinical Trials
  • 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
Preferred

Skills:
  • Budgeting
  • Clinical Trial Designs
  • Clinical Trials
  • 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
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Position Requirements
10+ Years work experience
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