Trial Delivery Manager

Johnson & Johnson Innovative Medicine; Imperia; Ibrido; EUR 55.000 - 75.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company is seeking a Trial Delivery Manager to manage study delivery and oversee trial activities across regions. The role requires a minimum of 4 years in clinical trials and a BS in Life Sciences. The ideal candidate will handle vendor management, support the feasibility strategy, and mentor team members. A flexible work model and a commitment to employee well-being make this role attractive. Join us in pioneering health solutions.

Servizi

Competitive salary

Flexible working environment

Career development opportunities

Competenze

• Minimum of 4 years clinical trial experience in Pharmaceutical or Healthcare industries.
• Experience supporting multiple aspects of a global clinical trial.
• Must possess excellent leadership skills and proven ability to foster team productivity.

Mansioni

• Create and update critical trial-specific documents.
• Manage vendor set up and oversee day-to-day study vendor activities.
• Responsible for country coordination of trial management activities.

Conoscenze

Clinical Trial Oversight

Vendor Management

Leadership skills

Analytical and decision-making skills

Formazione

BS degree in Life Sciences

Descrizione del lavoro

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At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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

Job Function

R&D Operations

Job Sub Function

Clinical Trial Project Management

Job Category

Professional

Locations

Beerse, Antwerp, Belgium; Breda, Netherlands; Duelmen, Germany; Imperia, Italy; Issy-les-Moulineaux, France; Leiden, Netherlands; Madrid, Spain; Warsaw, Masovian, Poland

Job Description

J&J IM - Trial Delivery Manager

J&J Flex – 3 days office/2 days remote – International Locations

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): Netherlands, Germany, France, Belgium (Requisition Number: R-045529); United Kingdom (Requisition Number: R-047381); United States (Requisition Number: XXXX). Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Company Overview

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

Position Summary

The Lead, 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).
• Manage vendor set up and manage 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

Required Minimum Education: BS degree or equivalent, preferred areas of study include Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)

Required Years Of Related Experience: Minimum of 4 years clinical trial experience in Pharmaceutical, Healthcare or related industries.

Required Knowledge and Experience

• 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 multi-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.

Other

Percentage Travelled: Travel up to 15‑20% of the time, defined by business needs.

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.

Office Location

We are pleased to announce that from mid‑2026, our offices in Wokingham and High Wycombe will move into a modern, state‑of‑the‑art Johnson & Johnson office in central Maidenhead, conveniently situated next to the train station.

Required Skills

Clinical Trial Oversight, Trial Management, Vendor Management

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)

Job Details

• Seniority level: Not Applicable
• Employment type: Full‑time
• Job function: Management and Manufacturing
• Industries: Pharmaceutical Manufacturing