Senior Clinical Research Associate

BDX

Milpitas, CA, USA
Base: $106,600.00 - $175,900.00 usd annual; bonus/...
Fully remote
Clinical site management and monitoring
Good clinical practice compliance
Cross-functional team collaboration
The Senior Clinical Research Associate plays a key role in managing clinical studies from initiation through close-out while ensuring compliance with applicable regulations and company standards

Job Summary

  • The Senior Clinical Research Associate plays a key role in managing clinical studies from initiation through close-out while ensuring compliance with applicable regulations and company standards.
  • BD is a global leader in medical technology committed to advancing health by fostering innovation, collaboration, and continuous learning within its teams.
  • This role offers a competitive salary range and emphasizes a culture of accountability, diversity, and employee development.

Matching Summary

The Senior Clinical Research Associate plays a key role in managing clinical studies from initiation through close-out while ensuring compliance with applicable regulations and company standards.

Salary

Base: $106,600.00 - $175,900.00 USD Annual; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Clinical site management and monitoring
  • Good Clinical Practice compliance
  • Cross-functional team collaboration
  • Clinical trial documentation and reporting
  • Use of EDC, CTMS, and eTMF systems
  • Travel up to 60% domestic and international

Nice-to-have

  • Mentoring and coaching junior team members
  • Experience with medical devices and diagnostic studies
  • Strong verbal and written communication skills
  • Proficiency in MS Windows applications
  • Ability to work independently and prioritize tasks
  • Participation in regulatory inspections and audits

Key Requirements

  • BS in healthcare or science related discipline
  • 5+ years clinical research associate experience
  • 2+ years medical device or diagnostic study experience preferred
  • Professional certification (e.g., ACRP, SOCRA, RAPS) desirable
  • Working knowledge of ICH GCP and relevant regulations
  • Experience with Ethics Review and submission management

Work Rights

Not specified

Tailored Resume

Cover Letter