Manager, Trial Delivery Management (H/F)

Biopharma Asia; Friauville; Hybrid; EUR 61,000 - 106,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Well-being reimbursement

Job summary

Johnson & Johnson in France is seeking a Manager, Trial Delivery Management (TDM) to lead end-to-end execution of study activities across global trials in a hybrid Issy-les-Moulineaux setting. You will oversee critical documents, vendor management, country/region delivery, risk reviews, and program-level training, ensuring Credo values and strong cross-functional collaboration.

A BS in Life Sciences and 8+ years in pharma with trial management leadership are required; we offer competitive

Qualifications

• BS degree in Life Sciences or equivalent.
• Minimum 8 years in Pharmaceutical, Healthcare or related industries.
• Experience in and knowledge of the pharmaceutical development process.
• Clinical research operational knowledge across multiple phases (Phase I-IV).
• Experience leading multiple aspects of a global clinical trial.

Responsibilities

• Create and update critical trial-specific documents (e.g., monitoring guidelines, informed consent forms, IMP-related documentation).
• Vendor setup and management of day-to-day study vendor activities, including SOW creation and budget oversight.
• Coordinate country/regional trial management activities and oversight (feasibility alignment, risk reviews).
• Support program-level compound training and collaboration with Clinical/CTL&D/Medical writing.
• Provide input into trial-level operational strategies and mitigate trial-related risks.
• Mentor and onboard new team members and support cross-functional collaboration.

Skills

Leadership

Budgeting

CTMS

Clinical Trial Management

Regulatory Compliance

Education

BS degree in Life Sciences

Job description

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:

Issy-les-Moulineaux, France

Job Description:

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

We are searching for the best talent for Manager, Trial Delivery Management (TDM) to be located in Issy les Molineaux, France (Hybrid). (Remote working will be considered on a case by case basis and with approval of the business).

There is a pre-identified candidate for this position, but all applications are welcome.

Position Summary:

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 Manager 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.

You will be responsible for:

Creating and updating 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).

Supporting development of program-level compound training, collaborating with Clinical / CTL&D / Medical writing.

Providing input into trial level operational strategies.

Resolve trial-related issues and mitigate trial-related risks.

Participating in process improvement activities at a trial, compound & cross-DU level, as needed.

Providing support during Health Authority inspections and on the identification of risks and mitigation plans at the program level for key issues.

Mentoring & supporting onboarding of new team members, particularly those in Trial Management.

Fostering employee engagement, inclusion, and Credo Behaviors.

Principal Relationships:

Internal: Trial Management Directors, Clinical Trial Leaders, Clinical Trial Assistants, Representatives of Delivery Operations, representatives of other GD Functions and Clinical Teams, representatives of Procurement

Are you ready to join our team? Then please read further!

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.

Benefits:

We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority, we have a flexible working environment as we value work-life balance. We offer career development opportunities for those who want to grow and be part of our organization.

Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will be considered for employment without regard to any other characteristic protected by law. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Required Skills:

Preferred Skills:

AI Judgement Integration, 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

The anticipated base pay range for this position is:

€61,300.00 - €105,570.00

Benefits:

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.