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**Job Function: **
R&D Operations
**Job Sub Function: **
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Leeds, West Yorkshire, United Kingdom
Job Description:
Johnson & Johnson announced plans to separate our Orthopedics business to establish a standalone orthopedics' company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.
Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.
DePuy Synthes (DPS) is recruiting for a Clinical Trial Leader. This role can be in Raynham, MA, West Chester, PA, Palm Beach Gardens, FL, or Warsaw, IN.
DePuy Synthes, the Orthopedics Company of Johnson & Johnson provides one of the most comprehensive orthopedics portfolios in the world. DePuy Synthes solutions, in specialties including joint reconstruction, trauma, craniomaxillofacial, spinal surgery and sports medicine, are designed to advance patient care while delivering clinical and economic value to health care systems worldwide. For more information, visit www.depuysynthes.com.
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):
US West Chester, PA, Palm Beach Gardens, FL or Warsaw, IN. - Req#: R-076520
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
About the Role
The Clinical Trial Leader (CTL) plays a meaningful role in advancing clinical research within DePuy Synthes. In this position, you will support the planning and execution of one or more clinical trials within the Clinical Operations organization while working closely with cross‑functional colleagues, clinical sites, and external partners.
This role is a great fit for someone who enjoys collaboration, values quality and compliance, and is motivated by contributing to innovative medical device development that improves patient outcomes.
Clinical Trial Execution
- Support the execution of company‑sponsored clinical trials within the Medical Device franchises, under appropriate supervision.
- Serve as the Clinical Trial Leader for assigned studies and actively participate as a member of the clinical study core team.
- Partner with Clinical Franchise colleagues and Clinical Business Strategy & Development Managers (BSDMs) to support study objectives.
- Help ensure trials are conducted in alignment with protocols, timelines, and regulatory requirements.
Operational Support & Collaboration
- Coordinate day‑to‑day operational activities for assigned studies, including site communication and vendor collaboration.
- May serve as a primary point of contact for clinical trial sites, fostering positive, productive relationships.
- Identify and address operational challenges with support from Clinical Management, escalating complex issues as appropriate.
- Track study budgets and support adherence to approved business plans.
- Assist with the implementation of clinical systems, tools, and process improvements.
Communication & Knowledge Sharing
- Share timely and accurate updates on study progress, milestones, and key events with internal stakeholders.
- Act as a reliable source of current project information when requested.
- Support publication activities and other study deliverables as needed.
Compliance, Quality & Ethics
- Support compliance with Good Clinical Practice (GCP), applicable regulations, and all Johnson & Johnson policies and procedures.
- Promote a culture of quality, safety, and ethical conduct aligned with the Johnson & Johnson Credo.
- Follow Health, Safety, and Environmental (HSE) guidelines in all activities.
- Ensure efficient and responsible use of resources while delivering high‑quality outcomes.
Additional Contributions
- May assist with complex or regulated clinical trials under the guidance of a Staff CTL, Clinical Trial Manager (CTM), or Senior CTM.
- Share business insights, risks, or opportunities with management as appropriate.
- Take on additional responsibilities as needed to support Clinical Operations and team goals.
Education & Experience
Required
- Bachelor’s degree or equivalent experience required; preferred fields include Life Sciences, Physical Sciences, Nursing, or Biological Sciences.
- 2–4 years of relevant professional experience, including exposure to clinical research, clinical operations, or regulated environments.
Preferred
- Experience in clinical trial management or related clinical research roles.
- Exposure to medical device development or clinical programs.
- Clinical or healthcare background.
- Industry certifications such as CCRA, RAC, or CDE.
Knowledge, Skills & Strengths
- Working knowledge of Good Clinical Practice (GCP) guidelines.
- Understanding of clinical regulations and standards across regions.
- Strong written and verbal communication skills, including technical documentation.
- Ability to collaborate effectively, build relationships, and contribute within cross‑functional teams.
- Organized, detail‑oriented, and comfortable managing multiple priorities.
- Demonstrates professionalism, integrity, and ethical decision‑making.
Why Join Us
At Johnson & Johnson and DePuy Synthes, you will be part of a collaborative, mission‑driven team focused on improving patient lives around the world. You will work in an environment that encourages innovation, supports professional growth, and values integrity, quality, and inclusion.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers . Internal employees contact AskGS to be directed to your accommodation resource.
**Required Skills: **
Preferred Skills:
Business Behavior, Clinical Research and Regulations, Clinical Trial Designs, Clinical Trial Management Systems (CTMS), Clinical Trials, Communication, Give Feedback, Laboratory Operations, Medical Knowledge, Mentorship, Problem Solving, Process Oriented, Professional Ethics, Project Integration Management, Project Management, Research and Development, Research Ethics