Job Description Summary

The Clinical Project Coordinator is responsible for delivering high quality and compliant support 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. The Clinical Project Coordinator will be responsible for the day-to-day operational support of assigned clinical studies, management of study supplies and investigational devices and administrative support for the Clinical Affairs team. The Clinical Project Coordinator may also support the review and development of essential clinical study documents.

Job Description

We are the makers of possible

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.

We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a makerof possible with us.

About the role:

As Clinical Project Coordinator, you will support the execution of clinical studies for BD Peripheral Intervention, ensuring regulatory compliance while managing daily operations, study supplies, and essential documentation.

Key responsibilities will include:

• Develop and maintain strong relationships with investigational site staff and study teams to support study deliverables.
• Ensure quality and compliance for activities performed for assigned clinical studies ensuring the highest standards for scientific quality, integrity and ethics are met
• Serve as a Clinical Product Management expert and resource for BD stakeholders, Investigators, and study site personnel.
• Support annual Sunshine Reporting activities and track transfers of value for clinical study supplies and investigational products, as appropriate.
• Support Clinical Project Management and/or Site Management & Monitoring with other administrative tasks
• Assist with study and site-level management of the Clinical Trial Management System (CTMS) to ensure that study and site details are current, accurate and complete.
• Develop and manage essential clinical study documents, including product management plans, forecasting templates, accountability logs, shipment and return forms, inspection records, and supplier contract requests.
• Support continuous improvement activities/initiatives and sharing of best practices.
• Communicate BD product complaints and other events/issues that inhibit safe and effective use of BD products and negatively impact data integrity.
• Participate in and/or support study-specific meetings including, but not limited to study team meetings, Clinical Product Management meetings, and vendor meetings.
• Perform general administrative functions (e.g., new hire onboarding tasks, IT requests, office supply orders, inventory management etc.), as needed.
• Provide critical thinking and support for issue escalation related to Clinical Product Management.
• Support processing and entry of clinical site payments/invoices within CTMS, as needed.

About you:

Education and experience required:

• Bachelor’s Degree (BS/BA) in life sciences
• 1+ years of experience in clinical research (medical device, pharmaceutical and/or biotechnology), with supply inventory management/shipment, or in a clinical setting
• Strong organizational skills, attention to detail, critical thinking, and analytical skills
• Able to manage, prioritize, and delegate multiple tasks
• Ability to travel up to 10%

Education and experience preferred:

• MA/MS
• Prior experience with clinical studies related to peripheral vascular diseases, end-stage kidney disease and/or oncology
• Experience with medical device studies
• Professional certification through one or more relevant associations (e.g., ACRP, SOCRA, etc.)

Why Join Us?

A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day.

You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time. And through the organization’s investment in BD University, you will continually level up your tech skills and expertise.

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.

To learn more about BD visit https://bd.com/careers

Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.

Required Skills

Optional Skills

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Primary Work Location

USA AZ - Tempe Headquarters

Additional Locations

Work Shift