Senior / Clinical Research Associate

Ivivamedical

Good clinical practice gcp knowledge
International conference on harmonization ich guidelines
Site monitoring visit execution
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out to ensure protocol adherence

Job Summary

  • The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out to ensure protocol adherence.
  • Candidates must work with sites to drive subject recruitment plans and manage ongoing project expectations through regular communication.
  • The position requires maintaining the Investigator's Site File in accordance with GCP and local regulatory requirements while resolving data queries.

Matching Summary

The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out to ensure protocol adherence.

Skills & Requirements

Must-have

  • Good Clinical Practice GCP knowledge
  • International Conference on Harmonization ICH guidelines
  • Site monitoring visit execution
  • Subject recruitment plan management
  • Trial Master File maintenance

Nice-to-have

  • Strong problem-solving skills
  • Effective time management abilities
  • Financial management experience
  • Collaborative team relationship building
  • Protocol training administration

Key Requirements

  • Bachelor's Degree in scientific discipline or health care
  • At least 1 year of on-site monitoring experience
  • Proficiency in Microsoft Word Excel and PowerPoint

Work Rights

Not specified

Tailored Resume

Cover Letter