Clinical Research Associate

539

Dublin, Ireland
Hybrid
Clinical study site management
Perform remote and on-site monitoring
Collect and review regulatory documentation
We are looking for a new colleague who is eager to learn and who does not shy away from a challenge

Job Summary

  • We are looking for a new colleague who is eager to learn and who does not shy away from a challenge.
  • You will be part of a fast-paced team full of positive and experienced people.
  • Perform clinical study site management and monitoring activities in compliance with International Conference on Harmonisation – Good Clinical Practice, Sponsor Standard Operating Procedures, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.

Matching Summary

We are looking for a new colleague who is eager to learn and who does not shy away from a challenge.

Skills & Requirements

Must-have

  • Clinical study site management
  • Perform remote and on-site monitoring
  • Collect and review regulatory documentation
  • ICH-GCP compliance
  • Site performance and compliance problem resolution

Nice-to-have

  • Eager to learn and embrace challenges
  • Fast-paced team environment
  • Positive and experienced colleagues
  • Work effectively in a multicultural environment

Key Requirements

  • Bachelor's degree or equivalent with 2+ years of site management experience
  • Associate degree/certificate with 5+ years healthcare experience including 2+ years site management
  • Ability to travel domestically 50% of working time
  • Hold a valid driver's license

Work Rights

Not specified

Tailored Resume

Cover Letter