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paradox

Senior Clinical Research Associate

Stryker
Remote, USA
Full-time
Mid · 2+ years experience
Remote
USD 83300-180400 yearly / year
Discovered 2 weeks ago

Full Job Posting

What you will do

  • Perform site monitoring and site management responsibilities through all phases of clinical study (e.g. site selection, site initiation, interim monitoring, and closeout)
  • Conduct site visits for all phases (site qualification, site initiation, interim monitoring, and closeout)
  • Ensure site compliance to clinical study protocol, applicable regulations and guidelines
  • Ensure data integrity by verifying data in case report forms against source documents
  • Identify and support site in addressing any noncompliance issues.
  • Collect and track regulatory documents, maintain trial master file (TMF) documentation and ensure accuracy
  • Communicate relevant updates to study core team

Required

Bachelor's level degree or equivalent in science or health care field

2+ years of relevant clinical research experience

Fundamental knowledge and good understanding of GCPs, clinical study development process, and logistics

Ability to apply ISO, FDA and related guidelines toward documentation

Preferred

Experience as a Clinical Research Coordinator, Clinical Trial Coordinator or Clinical Research Associate

CCRA Certification

Demonstrated independence in performing site monitoring (e.g. site selection, site initiation, interim monitoring and closeout visits) and site management activities

Posted Date: 10/09/2026 This role will be posted for a minimum of 3 days.

United States of America Pay Ranges

  • USN : $83,300 - $138,800 USD Annual
  • US5 : $87,500 - $145,700 USD Annual
  • US10 : $91,600 - $152,700 USD Annual
  • US15 : $95,800 - $159,600 USD Annual
  • US20 : $100,000 - $166,600 USD Annual
  • US30 : $108,300 - $180,400 USD Annual

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