Senior Clinical Trial Leader

Johnson & Johnson is separating its Orthopedics business into a standalone company, DePuy Synthes, in the next 18-24 months. The Senior Clinical Trial Leader (CTL) role will support clinical research for DePuy Synthes and be based in Warsaw, IN; West Chester, PA; Palm Beach Gardens, FL; or Raynham, MA. About The Role The Senior Clinical Trial Leader plays a key role in advancing clinical research within DePuy Synthes. You will support the planning and execution of one or more clinical trials within the Clinical Operations organization, collaborating closely with cross‑functional colleagues, clinical sites, and external partners. 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 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. Required 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. Preferred Skills Business Behavior, Clinical Research and Regulations, Clinical Trial Designs, Clinical Trial Management Systems (CTMS), Clinical Trial Management, Communication, Give Feedback, Laboratory Operations, Medical Knowledge, Mentorship, Problem Solving, Process Oriented, Professional Ethics, Project Integration Management, Project Management, Research and Development, Research Ethics. Pay Transparency The anticipated base pay range for this position is $92,000.00 - $148,350.00. This position is eligible to participate in the Company’s long‑term incentive program. Benefits Vacation – 120 hours per calendar year Sick time – 40 hours per calendar year; 48 hours for Colorado residents; 56 hours for Washington residents Holiday pay, including Floating Holidays – 13 days per calendar year Work, Personal and Family Time – up to 40 hours per calendar year Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child Bereavement Leave – 240 hours for an immediate family member; 40 hours for an extended family member per calendar year Caregiver Leave – 80 hours in a 52‑week rolling period Volunteer Leave – 32 hours per calendar year Military Spouse Time‑Off – 80 hours per calendar year 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. Your work will be in an environment that encourages innovation, supports professional growth, and values integrity, quality, and inclusion. Equal Opportunity Employer 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. Accommodation Policy Johnson & Johnson is committed to providing an inclusive interview process. If you are an individual with a disability and would like to request an accommodation, external applicants may contact us via Internal employees should contact AskGS to access resources. Additional general information on Company benefits is available at #J-18808-Ljbffr Johnson & Johnson