Clinical Safety Coordinator
Becton Dickinson · Tempe Headquarters
The apply link worked recently (not employer-confirmed).
Role summary
This Clinical Safety Coordinator role supports the day-to-day operations of clinical studies conducted by BD's Peripheral Intervention business unit. Responsibilities include maintaining compliance and quality standards across safety-related activities, coordinating between clinical sites and internal stakeholders, managing trial documentation, and preparing safety-related study documents. The position ensures studies meet regulatory requirements and organizational procedures.
What they're looking for
- Proficiency with Microsoft Office suite applications
- Strong written and oral communication skills
- Organizational skills with attention to detail
- Ability to manage multiple tasks and prioritize effectively
- Bachelor's degree in life sciences, nursing, or healthcare field
- 1+ years clinical research experience in medical device or pharmaceutical sectors
- Ability to travel up to 10% or more during peak periods
What you'll be doing
- Deliver operational support for Clinical Safety management activities in BDPI clinical studies
- Ensure quality and compliance with GCP, study protocols, and applicable regulations for safety activities
- Maintain Trial Master File documentation and conduct study-level audits for accuracy and completeness
- Develop and maintain relationships with investigational sites, medical monitors, and cross-functional teams
- Support creation of safety-related study documents including Clinical Safety Plans and committee charters
Privacy & handoff
This role links to Becton Dickinson's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.