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 management processes
Protocol compliance monitoring
Electronic data capture (edc) systems
Johnson & Johnson is pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease

Job Summary

  • Johnson & Johnson is pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
  • The Clinical Research Associate II is responsible for facilitating setup, activation, maintenance, and closure of global clinical trials while ensuring compliance with protocols and clinical objectives.
  • Employees are eligible for comprehensive time off benefits including vacation, sick time, parental leave, bereavement leave, caregiver leave, volunteer leave, and military spouse time-off.

Matching Summary

Johnson & Johnson is pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.

Salary

Base: $87,000.00 - $140,300.00; Bonus/Equity: Not specified; Benefits: Vacation, sick time, parental leave, bereavement leave, caregiver leave, volunteer leave, military spouse time-off

Skills & Requirements

Must-have

  • Clinical trial management processes
  • Protocol compliance monitoring
  • Electronic Data Capture (EDC) systems
  • Clinical data quality assurance
  • Regulatory document coordination
  • Safety report tracking
  • Remote work capability

Nice-to-have

  • Peripheral and coronary artery disease knowledge
  • Clinical research certification
  • Study site training delivery
  • Cross-functional team collaboration
  • Audit preparedness
  • Fast-paced environment adaptability
  • Strong verbal and written communication

Key Requirements

  • Bachelor’s degree in scientific field
  • Minimum 2 years clinical research experience
  • Knowledge of GCP, FDA, ISO regulations
  • Ability to travel 10-20% domestically and internationally
  • ACRP or SOCRA clinical research certification preferred

Work Rights

Not specified

Tailored Resume

Cover Letter