Cardio Medical Device Clinical Research Associate

ICON Strategic Solutions

California

On-site

USD 90,000 - 120,000

Full time

6 days ago
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Benefits offered by this job

Annual leave
Health insurance
Retirement planning
Employee Assistance Program
Life assurance
Flexible benefits

Job summary

ICON is seeking an experienced regional Clinical Research Associate (CRA) based in California to monitor cardiovascular device studies within a sponsor team. You’ll act as the primary site contact, conduct visits, ensure regulatory compliance, and maintain CTMS/eTMF documentation while supporting recruitment and safety reporting.

The ideal candidate has 3+ years of on-site monitoring in pharma or CRO, with cardiovascular device experience preferred.

Qualifications

  • Requires 3+ years of on-site monitoring experience in pharma or CRO
  • Cardiovascular medical device monitoring experience preferred
  • Knowledge of ICH-GCP and regulatory requirements essential

Responsibilities

  • Serve as the primary site sponsor contact and monitor study progress
  • Conduct site visits including selection, initiation, routine monitoring and close-out
  • Ensure site compliance with ICH-GCP, SOPs and health regulations
  • Maintain documentation in CTMS and eTMF
  • Monitor patient safety and adverse event reporting
  • Support site patient recruitment and retention at the site level
  • Collaborate with cross-functional teams across CTAs, LTMs, and CTMs

Skills

On-site monitoring
Cardiovascular device knowledge
ICH-GCP
CTMS
eTMF

Education

Bachelor’s degree in Life Sciences or equivalent
RN license

Tools

CTMS
eTMF

Job description

ICON is seeking an experienced regional Clinical Research Associate (CRA) based in California to monitor cardiovascular device studies within a sponsor team. You’ll act as the primary site contact, conduct visits, ensure regulatory compliance, and maintain CTMS/eTMF documentation while supporting recruitment and safety reporting.

The ideal candidate has 3+ years of on-site monitoring in pharma or CRO, with cardiovascular device experience preferred.

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