Clinical Safety Specialist — Medical Device Studies

Becton, Dickinson and Company; Tempe (AZ); On-site; USD 85,000 - 110,000; Full time

Job summary

Becton, Dickinson, and Company (BD) is seeking a Clinical Safety Coordinator to deliver day-to-day operational support for the Clinical Safety team across BDPI studies. You will help ensure scientific quality, integrity, and ethics, aligning with GCP and global procedures.

The role requires collaboration with investigators, medical monitors, and BD stakeholders, plus maintaining TMF documentation and safety-related reports. On-site work in Tempe, with potential travel up to 10%.

Qualifications

• Bachelor’s Degree in life sciences or related field; 1+ year in clinical research.
• Experience with clinical safety management or medical device safety reporting.
• Proficiency with Microsoft Office and collaboration tools.
• Strong organizational, communication, and analytical skills.
• Ability to travel up to 10% (more during peak times).

Responsibilities

• Provide operational support for Clinical Safety management activities.
• Ensure quality and compliance with GCP and BD procedures.
• Maintain relationships with investigators and cross-functional study teams.
• Facilitate communication between clinical sites and BD stakeholders.
• Support TMF maintenance and audits to ensure audit readiness.
• Prepare safety-related study documents and tracking reports.
• Support safety training and invoicing for safety vendors.
• Participate in safety meetings and vendor coordination.

Skills

Microsoft Suite proficiency

Interpersonal communication

Organizational skills

Multitasking / time management

Travel readiness

Education

Bachelor's Degree in life sciences or related field

Tools

Veeva Vault

CTMS

CDMS

eTMF

Job description

Becton, Dickinson, and Company (BD) is seeking a Clinical Safety Coordinator to deliver day-to-day operational support for the Clinical Safety team across BDPI studies. You will help ensure scientific quality, integrity, and ethics, aligning with GCP and global procedures.

The role requires collaboration with investigators, medical monitors, and BD stakeholders, plus maintaining TMF documentation and safety-related reports. On-site work in Tempe, with potential travel up to 10%.