Clinical Study Operations Specialist

BD; Tempe (AZ); On-site; USD 60,000 - 86,000; Full time

Job summary

BD is seeking a Clinical Project Coordinator to deliver high-quality, compliant support for BD Peripheral Intervention clinical studies. You will manage day-to-day operational support, study supplies, and site coordination to ensure adherence to GCP and BD procedures.

The role requires collaboration with investigators and BD stakeholders, strong documentation practices, and the ability to travel up to 10%. A BS/BA in life sciences and 1+ years of clinical research experience are preferred, with

Qualifications

• Proficiency with Microsoft Suite tools (Outlook, Word, Excel, PowerPoint, OneNote, To-Do, SharePoint).
• Strong interpersonal and communication/presentation (oral and written) skills.
• Strong organizational skills, attention to detail, critical thinking and analytical skills.
• Able to manage and delegate multiple tasks and prioritize importance of tasks/projects.
• Ability to travel up to 10% (or more during peak times).

Responsibilities

• Provide operational support for BDPI clinical studies to enable successful completion of study objectives and deliverables.
• Ensure quality and compliance for activities performed for assigned clinical studies ensuring the highest standards for scientific quality, integrity and ethics.
• Prepare and ship clinical study supplies and investigational products to domestic and international locations.
• Manage inventory and accountability of clinical study supplies and investigational products.
• 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.

Skills

MS Office

Interpersonal skills

Organizational skills

Communication skills

Willingness to travel

Education

BS/BA in life sciences

Tools

Veeva Vault

Job description

BD is seeking a Clinical Project Coordinator to deliver high-quality, compliant support for BD Peripheral Intervention clinical studies. You will manage day-to-day operational support, study supplies, and site coordination to ensure adherence to GCP and BD procedures.

The role requires collaboration with investigators and BD stakeholders, strong documentation practices, and the ability to travel up to 10%. A BS/BA in life sciences and 1+ years of clinical research experience are preferred, with