Clinical Research Associate Ii- Shockwave Medical

J&J FAMILY OF COMPANIES

Santa Clara, California, United States of America
Base: $87,000.00 - $140,300.00; bonus/equity: elig...
Fully remote
Clinical trial project management
Compliance with protocol and regulations
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 global clinical trial setup, activation, maintenance, and closure while ensuring compliance with protocols and clinical objectives.
  • Employees are eligible for comprehensive benefits including retirement plans, vacation, sick time, parental leave, and various other time-off programs.

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: Eligible for long-term incentive program; Benefits: Retirement plans, vacation, sick leave, parental leave, and other paid time off

Skills & Requirements

Must-have

  • Clinical trial project management
  • Compliance with protocol and regulations
  • Electronic Data Capture (EDC) systems
  • Clinical data quality assurance
  • Site visit coordination and monitoring
  • Regulatory document management

Nice-to-have

  • Peripheral and coronary artery disease knowledge
  • Clinical research certification (ACRP or SOCRA)
  • Strong verbal and written communication skills
  • Ability to work independently and in teams
  • Flexibility to changing requirements

Key Requirements

  • Bachelor’s degree in science or healthcare
  • Minimum 2 years medical device clinical research experience
  • Working knowledge of GCP, FDA, ISO regulations
  • Ability to travel 10-20% domestically and internationally
  • Preferred clinical research certification (ACRP or SOCRA)

Work Rights

Not specified

Tailored Resume

Cover Letter