Clinical Research Associate Ii- Shockwave Medical

Johnson & Johnson

Santa Clara, California, United States of America
Base: $87,000.00 - $140,300.00; bonus/equity: not ...
Fully remote
Clinical trial setup and maintenance
Ensure protocol compliance
Data quality and discrepancy interpretation
The Clinical Research Associate II (CRA II) is responsible for facilitating in-house set up, activation, maintenance and closure of global clinical trials while gaining experience in clinical trial management processes

Job Summary

  • The Clinical Research Associate II (CRA II) is responsible for facilitating in-house set up, activation, maintenance and closure of global clinical trials while gaining experience in clinical trial management processes.
  • The CRA II will work closely with Investigators, Site Personnel and Vendors to ensure compliance with protocol and overall clinical objectives.
  • Johnson & Johnson is hiring for a Clinical Research Associate II– Shockwave Medical to join our team. The position is FULLY REMOTE and can sit anywhere in the US.

Matching Summary

The Clinical Research Associate II (CRA II) is responsible for facilitating in-house set up, activation, maintenance and closure of global clinical trials while gaining experience in clinical trial management processes.

Salary

Base: $87,000.00 - $140,300.00; Bonus/Equity: Not specified; Benefits: Eligible for Company's consolidated retirement plan (pension) and savings plan (401(k)), long-term incentive program, vacation, sick time, holiday pay, Work/Personal/Family Time, Parental Leave, Bereavement Leave, Caregiver Leave, Volunteer Leave, Military Spouse Time-Off

Skills & Requirements

Must-have

  • Clinical trial setup and maintenance
  • Ensure protocol compliance
  • Data quality and discrepancy interpretation
  • Interaction with site personnel and vendors
  • Regulatory document review

Nice-to-have

  • Develops basic disease knowledge
  • Team player with flexibility
  • Fast-paced environment adaptability

Key Requirements

  • Minimum 2 years medical device industry experience
  • Bachelor's degree in science or healthcare
  • Working knowledge of GCP, FDA, ISO regulations
  • Experience with EDC Data Management Systems

Work Rights

Not specified

Tailored Resume

Cover Letter