Onsite Medical Affairs Senior Manager, Clinical Programs

BD

Franklin Lakes (NJ)

On-site

USD 172,000 - 275,000

Full time

14 days+

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Benefits offered by this job

Health benefits
401(k) Plan
Paid time off
Dental coverage

Job summary

BD is a leading global medical technology company. We are seeking an experienced leader for Program/Clinical Trial activities based in Franklin Lakes, NJ, onsite daily.

The role involves directing EP ASCP/ASVP staff, hiring and managing personnel, ensuring regulatory compliance, and coordinating with IRB/EC and project teams. Ideal candidates have a clinical background (RN/PA/NP), a science degree, 5+ years in clinical trials, and strong program management experience.

Qualifications

  • Licensed Healthcare Practitioner (RN/PA/NP) with a science degree
  • Minimum 5 years in human clinical trials, GCP experience preferred
  • Minimum 5 years in Program Management and people management

Responsibilities

  • Provide leadership and guidance to EP ASCP and ASVP staff as directed by VP, EP
  • Hire, evaluate and manage EP associates, contractors and/or vendor personnel
  • Support expansion of Program activities to global or new locations
  • Oversee submissions with the ASCP IRB and EC
  • Provide monitoring expertise and manage assigned clinical site(s)/project(s)
  • Ensure site staff follow protocols and regulatory standards (GCP/ISO)
  • Maintain audit-ready regulatory files for assigned sites/projects
  • Onsite daily presence in Franklin Lakes, NJ

Skills

Leadership
Project management
Regulatory compliance
Clinical trials
Communication
Team management

Education

Licensed Healthcare Practitioner (RN/PA/NP)
Bachelor’s degree in Science-related field
Clinical trial management certification

Job description

BD is a leading global medical technology company. We are seeking an experienced leader for Program/Clinical Trial activities based in Franklin Lakes, NJ, onsite daily.

The role involves directing EP ASCP/ASVP staff, hiring and managing personnel, ensuring regulatory compliance, and coordinating with IRB/EC and project teams. Ideal candidates have a clinical background (RN/PA/NP), a science degree, 5+ years in clinical trials, and strong program management experience.

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