Clinical Project Manager

Responsibilities

• Develops and authors clinical research protocols, ensuring alignment with study objectives, regulatory requirements, and scientific standards.
• Manages essential study documents, maintains the trial master file, supports approvals, and leads final study reporting and closeout activities for complex trials.
• Trains and manages CRA teams to ensure high-quality monitoring, while overseeing external vendors (e.g., CROs, labs) to maintain performance and compliance.
• Leads budget and timeline development in collaboration with core teams, oversees site selection and training, and ensures efficient study execution and status reporting.
• Works closely with clinical data management and biostatistics teams to design case report forms, support data cleaning, and contribute to accurate study analysis.
• Minimum Requirements:
• Bachelor degree required. Education and experience sufficient to contribute within local work unit with limited supervision. Preferred education/experience areas include the life sciences or other relevant technical area, such as clinical trials, Regulatory Affairs, or Quality.
• Minimum 3 years of recent experience in clinical study management with pharmaceutical, device, or CRO company.
• Project management skills required to include the use of a formal process and system for planning and tracking ongoing progress of clinical projects
• Vendor management experience required.
• The Clinical Project Manager is expected to travel approximately 30% of the time, US and Internationally.
• Preferred Requirements:
• Proficiency with MS Project highly preferred,
• RN, RPh, Veterinary Technician/Technologist or Medical Technician/Technologist licensing or degree preferred.
• Professional certification through one or more relevant associations (e.g., ACRP, SOCRA, RAPS) desirable.
• Knowledge and experience of Good Clinical Practice (GCP) and ICH requirements required. Knowledge of additional/local regulations a plus.
• Why Join Us?
• We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
• To learn more about BD visit https://bd.com/careers .
• Required Skills
• Optional Skills
• .
• Primary Work Location
• USA NJ - Franklin Lakes
• Additional Locations
• Work Shift
• At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a

Benefits

Additional Information

We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. Job Description Clinical Project Manager serves as a study and project manager for studies of moderate to high complexity from protocol development through study conduct and study closeout in compliance with Good Clinical Practices, and all National and Local Regulations.

Your Match

How well this role fits your profile.

Company Intel

What employees say

Worked at Becton Dickinson? Share your experience