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Senior Clinical Project Coordinator
BDClinical Project Coordinator at BD providing operational support for clinical studies. Preparing and shipping clinical study supplies while ensuring compliance with regulations and guidelines.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Clinical Product Management and operational support for clinical studies, ensuring compliance with study objectives and deliverables. Proficient in managing trial master files and conducting audits to maintain accuracy and readiness.
Highest-signal resume keywords
Clinical Research ExperienceTrial Master File MaintenanceSupply Inventory ManagementMicrosoft Suite ProficiencyOrganizational Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical ResearchTrial Master File MaintenanceSupply Inventory ManagementAudit PreparationData Analysis
Soft Skills
Attention to DetailCritical ThinkingAnalytical SkillsTask ManagementDelegation
Tools & Technologies
Microsoft OutlookMicrosoft WordMicrosoft ExcelMicrosoft PowerPointMicrosoft OneNoteMicrosoft To-DoMicrosoft SharePoint
Industry Keywords
Clinical StudiesMedical DevicePharmaceuticalBiotechnologyOperational Support
About the role
Key responsibilities & impact- Provide operational support for BDPI clinical studies to enable successful completion of study objectives and deliverables.
- Prepare and ship clinical study supplies and investigational products from BD Peripheral Intervention’s headquarters to domestic and international locations.
- Serve as a Clinical Product Management expert and resource for BD stakeholders, Investigators, and study site personnel.
- Support Clinical Project Management and/or Site Management & Monitoring with other administrative tasks as needed.
- Trial Master File (TMF) maintenance and perform study and/or site-level audits to ensure that study files are current, accurate, complete and audit-ready.
Requirements
What you’ll need- Bachelor’s Degree (BS/BA) in life sciences or equivalent combination of training and experience (MA/MS preferred)
- 1+ years of experience in clinical research (medical device, pharmaceutical and/or biotechnology), with supply inventory management/shipment, or in a clinical setting
- Proficiency with Microsoft Suite tools (Outlook, Word, Excel, PowerPoint, OneNote, To-Do, SharePoint, etc.)
- Strong organizational skills, attention to detail, critical thinking and analytical skills
- Able to manage and delegate multiple tasks and prioritize importance of tasks/projects
Benefits
Comp & perks- Comprehensive Total Rewards program
- Reward and recognition opportunities