Lead, Trial Delivery Management

6010-Biosense Webster Inc. Legal Entity

Breda

On-site

EUR 64,000 - 103,000

Full time

5 days ago
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Benefits offered by this job

Annual bonus
Vacation days
Well-being reimbursement

Job summary

Johnson & Johnson seeks an experienced Clinical Trial Project Manager to lead multinational trial management, coordinating country-level activities, feasibility, and vendor setup across Beerse, Breda, and other locations.

Required 4+ years in clinical trials, BS in Life Sciences, and strong leadership, communication, and budget-management skills; travel up to 15–20% is expected.

Qualifications

  • BS degree in Life Sciences; preferred fields include Biology, Chemistry, Biochemistry, Nursing, Pharmacy.
  • Minimum 4 years of clinical trial experience in pharmaceutical or healthcare industries.
  • Experience in global multi-phase trials (Phase I-IV) and ability to manage multiple aspects.
  • Strong leadership, communication, and financial management skills.

Responsibilities

  • Create and update trial documents (Monitoring Guidelines, ICF, IMP related docs).
  • Manage vendor setup and day-to-day study vendor activities.
  • Coordinate country-level trial management and risk reviews across regions.
  • Support program-level training with Clinical/CTL&D/Medical Writing.

Skills

Leadership
Project management
Communication
Analytical thinking

Education

BS degree in Life Sciences

Tools

CTMS

Job description

Company Overview

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow,and profoundly impact health for humanity.Learn more at jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Details

Job Function: R&D Operations

Job Sub Function: Clinical Trial Project Management

Job Category: Professional

All Job Posting Locations: Beerse, Antwerp, Belgium, Breda, Netherlands, Madrid, Spain, Milano, Italy, Warsaw, Masovian, Poland

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s): High Wycombe, United Kingdom - Requisition Number: R-096653 Spring House, PA, Titusville, NJ United States - Requisition Number: R-098245 Beerse, Belgium, Breda, Netherlands, Warsaw, Poland, Madrid, Spain, Milan, Italy - Requisition Number: R-098254 Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Principal Responsibilities
  • Create and update critical trial-specific documents (e.g., Monitoring Guidelines, Informed Consent Form, Investigational Medicinal Product [IMP] related documentation).
  • Manage vendor set up and management of day-to-day study vendor activities, including set-up, SOW creation and budget oversight.
  • Responsible for country / regional coordination of trial management activities and oversight (e.g., aligns feasibility strategy with local teams, perform country-level risk reviews, aware of all projects conducted across countries).
  • Support development of program-level compound training, collaborating with Clinical / CTL&D / Medical writing.
  • Provide input into trial level operational strategies.
  • Resolve trial-related issues and mitigate trial-related risks.
  • Participate in process improvement activities at a trial, compound & cross-DU level, as needed.
  • Provide support during Health Authority inspections and on the identification of risks and mitigation plans at the program level for key issues.
  • Mentor & support onboarding of new team members, particularly those in Trial Management.
Education and Experience Requirements
  • BS degree or equivalent, preferred areas of study include Life Sciences (Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)
  • Required Years of Related Minimum of 4 years clinical trial experience in Pharmaceutical, Healthcare or related industries.
  • Clinical research operational knowledge and experience across multiple phases of studies (Phase I-IV); must have the ability to manage multiple aspects of execution of a clinical trial.
  • 2-3 years’ experience supporting multiple aspects of a global clinical trial.
  • Must possess excellent leadership skills and proven ability to foster team productivity and cohesiveness.
  • Experience leading without authority and in muti-functional matrixed and global environments.
  • Excellent decision-making, analytical and strong financial management skills are essential to this position.
  • Operate and execute with limited supervision.
  • Experience mentoring/coaching others.
  • Strong project planning/management, communication and presentation skills are required.
  • Travel up to 15-20% of the time, defined by business needs.
Preferred Skills
  • Analytical Reasoning
  • Clinical Research and Regulations
  • Clinical Trial Designs
  • Clinical Trial Management Systems (CTMS)
  • Clinical Trials
  • Communication
  • Data Savvy
  • Laboratory Operations
  • Organizing
  • Problem Solving
  • Productivity Planning
  • Professional Ethics
  • Project Integration Management
  • Quality Assurance (QA)
  • Regulatory Compliance
  • Research and Development
  • Research Ethics
  • Standard Operating Procedure (SOP)
Salary
  • The anticipated pay range for this position, in the primary posting location, is: €64,000.00 - €103,040.00
  • The anticipated pay ranges for additional locations are:
  • Spain – The anticipated base pay range for this position is 55,400 – 87,860 EUR
  • Italy – The anticipated base pay range for this position is 48,600 – 77,395 EUR
  • Poland – The anticipated base pay range for this position is 210,000 – 402,500 PLN
  • Belgium – The anticipated base pay range for this position is 72,500 – 115,230 EUR
Benefits
  • An annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions.
  • Vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health.
  • Service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans.
  • *This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.
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