Manager, Trial Delivery Management

6010-Biosense Webster Inc. Legal Entity; Geel; Sur place; EUR 80 000 - 138 000; Plein temps

Avantages offerts par ce poste

Annual bonus

Vacation days

Parental leave

Bereavement leave

Caregiver leave

Volunteer leave

Well-being reimbursement

Health insurance

Service recognition awards

Insurance plans

Résumé du poste

Johnson & Johnson is seeking a Manager, Trial Delivery Management (TDM) to oversee study-level activities across multiple countries. You will create and update trial documents, oversee vendors, manage feasibility alignment with local teams, and mitigate risks to ensure timely trial delivery.

The role requires 8+ years in pharma/healthcare, strong leadership, and experience in global clinical trials (Phase I–IV).

Qualifications

• BS degree or equivalent in Life Sciences (Life Sciences fields such as Biology, Chemistry, Biochemistry, Nursing, Pharmacy).
• Minimum of 8 years in Pharmaceutical/Healthcare or related industries.
• Experience in pharmaceutical development processes and clinical trial execution across multiple phases (I-IV).
• 2-3 years’ experience leading multiple aspects of a global clinical trial.
• Ability to manage all aspects of trial execution with limited supervision.

Responsabilités

• Create and update critical trial-specific documents (Monitoring Guidelines, Informed Consent Form, IMP documentation).
• Vendor setup and management of day-to-day study vendor activities, including SOW creation and budget oversight.
• Coordinate country/regional trial management activities, align feasibility strategy with local teams, perform country-level risk reviews.
• Support development of program-level compound training with Clinical/CTL&D Medical writing.

Connaissances

Analytical Reasoning

Budgeting

Clinical Trials

Contract Management

Execution Focus

Decision Making

Research Ethics

SOP

Laboratory Operations

Mentorship

Process Improvements

Project Integration Management

Research and Development

CTMS

Formation

BS degree or equivalent in Life Sciences

Outils

CTMS

Description du poste

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 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

Job Description:

About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine

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-096646 Spring House, PA, Titusville, NJ United States - Requisition Number: R-098278 Warsaw, Poland, Madrid, Spain, Milan, Italy - Requisition Number: R-098282 Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

The Manager, Trial Delivery Management (TDM) is responsible for the execution of study-level activities, creating and updating trial-specific documents, vendor oversight & delivery, compound training, and other activities. The TDM is responsible for country and regional oversight of local operational delivery, including the alignment of the feasibility strategy and target setting, risk reviews and local challenges that could impact overall study delivery.

Principal Responsibilities:

• Create and update critical trial-specific documents (e.g., Monitoring Guidelines, Informed Consent Form, Investigational Medicinal Product [IMP] related documentation).
• 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.

Additional Responsibilities may Include:

• 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.
• Foster employee engagement, inclusion, and Credo Behaviors.

Education and Experience Requirements:

• BS degree or equivalent, preferred areas of study include Life Sciences (Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy))
• Minimum of 8 years in Pharmaceutical, Healthcare or related industries.
• Experience in and knowledge of the pharmaceutical development process.
• Clinical research operational knowledge and experience across multiple phases of studies (Phase I-IV); must have the ability to manage all aspects of execution of a clinical trial.
• 2-3 years’ experience leading multiple aspects of a global clinical trial.
• Must possess excellent leadership skills and proven ability to foster team productivity and cohesiveness.
• Experience of 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 Related Industry Experience:

• Pharmaceutical
• Biopharmaceutical
• Biotechnology

Preferred Skills:

• Analytical Reasoning
• Budgeting
• Clinical Trial Management Systems (CTMS)
• Clinical Trials
• Compliance Management
• Contract Management
• Execution Focus
• Fact-Based Decision Making
• Laboratory Operations
• Mentorship
• Process Improvements
• Project Integration Management
• Research and Development
• Research Ethics
• Standard Operating Procedure (SOP)
• Technical Credibility

Anticipated Pay Range:

The anticipated pay range for this position, in the primary posting location, is: €79,800.00 - €137,770.00

The anticipated pay ranges for additional locations are: Spain – The anticipated base pay range for this position is 61,800 – 106,260 EUR Italy – The anticipated base pay range for this position is 56,100 – 96,945 EUR Poland – The anticipated base pay range for this position is 251,000 – 483,000 PLN Belgium – The anticipated base pay range for this position is 79,800 – 137,770 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
• employees - and in some location’s eligible dependents - can participate in several insurance plans.

In addition to base pay, we offer the following 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. Moreover, we offer 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. We also offer 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. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers. *This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.

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 https://www.jnj.com/.