Clinical Trial Manager

Johnson & Johnson Innovative Medicine•Warsaw, IN

About The Position

DePuy Synthes (DPS) is recruiting for a Clinical Trial Manager. 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. About the Role The Clinical Trial Manager (CTM) supports the planning and execution of company‑sponsored clinical trials within the Clinical Operations organization. This role partners closely with Clinical Franchise teams and cross‑functional stakeholders to ensure studies are delivered with quality, efficiency, and regulatory compliance. The Clinical Trial Manager also fosters strong working relationships across the organization and may provide leadership and oversight to Clinical Trial Leaders. This role is ideal for a collaborative clinical research professional who values continuous improvement and enjoys contributing to patient‑focused innovation in a regulated environment.

Requirements

Bachelor’s degree or equivalent experience required; preferred fields include Life Sciences, Physical Sciences, Nursing, Biological Sciences, or related disciplines.
4–6 years of relevant professional experience in clinical research, clinical operations, or a regulated medical device or pharmaceutical environment.
Demonstrated experience managing clinical trial operations, study execution, or cross‑functional clinical initiatives.
Strong working knowledge of Good Clinical Practice (GCP) and applicable regulatory requirements.
Proven ability to manage multiple priorities and deliver results in a matrixed environment.
Effective written and verbal communication skills with the ability to present information clearly to diverse audiences.

Nice To Haves

Experience leading or supervising Clinical Trial Leaders or study team members.
Medical device clinical trial experience.
Clinical or healthcare background.
Industry certifications such as CCRA, RAC, or CDE.

Responsibilities

Lead operational execution of assigned clinical trials and programs within Clinical Operations.
Serve as a core team member for clinical studies and programs, supporting alignment with Clinical Franchise priorities.
Act as a liaison or back‑up liaison to the Clinical Franchise and Clinical Business Strategy & Development Managers (BSDMs).
Serve as a point of contact for clinical trial sites, supporting clear, consistent communication.
Manage all operational activities across assigned studies, including planning, execution, tracking, and close‑out.
Independently address day‑to-day operational issues; escalate complex challenges when appropriate.
Plan, track, and manage study budgets to support adherence to approved business plans.
Manage study resources to ensure high‑quality deliverables while maintaining operational efficiency.
Provide direction and coaching to Clinical Trial Leaders, as applicable.
Partner with cross‑functional stakeholders including Quality, Regulatory, Supply Chain, and Franchise teams.
Communicate key clinical data, milestones, and risks to internal stakeholders.
Serve as a reliable and knowledgeable resource for study information.
Support implementation and adoption of new clinical systems, tools, and processes.
Contribute to clinical publications and study deliverables, as required.
Identify and support opportunities to improve consistency, quality, and efficiency in clinical operations.
Ensure studies are conducted in compliance with Good Clinical Practice (GCP), applicable regulations, and Johnson & Johnson policies.
Support Health, Safety, and Environmental (HSE) practices across all activities.
Model behaviors aligned with the Johnson & Johnson Credo values.