Bachelor's degree3+ years clinical study managementGCP / ICH knowledgeProtocol developmentProject managementVendor / CRO managementTrial master file managementCRA team managementMS Project proficiencyClinical certification (ACRP/SOCRA/RAPS)RN / RPh / Medical Technologist license30% travel availability
Job Description
BD is seeking a Clinical Project Manager to oversee clinical research studies from protocol development through closeout, ensuring compliance with Good Clinical Practices and regulations. The role involves managing study documentation, leading CRA teams, coordinating with vendors, managing budgets and timelines, and collaborating with clinical data and biostatistics teams. The position requires 3+ years of clinical study management experience and involves approximately 30% travel.
Overview
BD (Becton, Dickinson, and Company) is one of the largest global medical technology companies in the world. The Clinical Project Manager serves as a study and project manager for studies of moderate to high complexity, from protocol development through study conduct and closeout, in compliance with Good Clinical Practices and all applicable regulations.
Responsibilities
•Develop and author clinical research protocols, ensuring alignment with study objectives, regulatory requirements, and scientific standards.
•Manage essential study documents, maintain the trial master file, support approvals, and lead final study reporting and closeout activities for complex trials.
•Train and manage CRA teams to ensure high-quality monitoring, while overseeing external vendors (e.g., CROs, labs) to maintain performance and compliance.
•Lead budget and timeline development in collaboration with core teams, oversee site selection and training, and ensure efficient study execution and status reporting.
•Work 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's degree required; preferred in 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 a pharmaceutical, device, or CRO company.
•Project management skills required, including use of a formal process and system for planning and tracking ongoing progress of clinical projects.
•Vendor management experience required.
•Knowledge and experience of Good Clinical Practice (GCP) and ICH requirements required.
•Willingness 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 of additional or local regulations a plus.
Compensation
•Salary Range: $110,200 - $176,400 USD Annual
•Annual bonus eligibility
•Comprehensive benefits including medical, dental, vision, life insurance, disability coverage, 401(k), paid parental leave, tuition reimbursement, and more.
Work Location
Primary location: Franklin Lakes, NJ. Minimum 4 days of in-office presence per week required.
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