We are the people who give possibilities purposeBD 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 DescriptionPosition Summary: The Clinical Safety Coordinator is responsible for delivering high quality and compliant day-to-day operational support for the Clinical Safety team for clinical studies e.g., EFS/FIH, IDE, Post-Market sponsored by the BD Peripheral Intervention business unit to ensure they meet the highest standards for scientific quality, integrity and ethics and are conducted in accordance with BD global clinical procedures, study protocols, GCP and all applicable regulations. Key Job Responsibilities: Provide operational support for Clinical Safety management activities for BDPI clinical studies to enable successful completion of study objectives and deliverables. Ensure quality and compliance for safety-related activities performed for assigned clinical studies ensuring the highest standards for scientific quality, integrity and ethics are met and that these are conducted in accordance with BD global clinical procedures, study protocols, GCP and all applicable regulations. Develop and maintain strong relationships with investigational site staff, HCP consultants e.g., Medical Monitors, CEC/DMC members, and cross-functional study teams to support Clinical Safety deliverables. Facilitate communication between clinical sites and BD stakeholders e.g., PMs, CRAs, as needed. Support Trial Master File TMF maintenance for Clinical Safety documentation and perform study and/or site-level audits to ensure that study files are current,
Visit
Careersaas to find millions of new and unfilled roles, including thousands of remote and hybrid positions.
