Trial Delivery Manager - Global Clinical Ops

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

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