Clinical Research Associate

Ivivamedical

**
Gcp and ich guidelines knowledge
On-site monitoring experience
Protocol adherence and compliance
** Ivivamedical is seeking experienced Clinical Research Associates to monitor and manage clinical trials, ensuring compliance with protocols and regulatory requirements. The role emphasizes strong communication with site staff and internal teams, requiring a minimum of one year of on-site monitoring experience. **

Job Summary

  • The role involves conducting selection, initiation, monitoring, and close-out visits to ensure study sites operate in compliance with protocols and GCP/ICH guidelines.
  • Candidates will work closely with site staff to develop subject recruitment plans and provide protocol-specific training to personnel.
  • The position requires maintaining essential documents in the TMF and verifying ISF compliance while documenting all site management activities through timely reports.

Matching Summary

Match Score: 75

** Ivivamedical is seeking experienced Clinical Research Associates to monitor and manage clinical trials, ensuring compliance with protocols and regulatory requirements. The role emphasizes strong communication with site staff and internal teams, requiring a minimum of one year of on-site monitoring experience. **

Skills & Requirements

Must-have

  • GCP and ICH guidelines knowledge
  • On-site monitoring experience
  • Protocol adherence and compliance
  • Site recruitment plan development
  • Essential document maintenance

Nice-to-have

  • Strong cross-functional collaboration
  • Excellent problem-solving abilities
  • Effective communication skills
  • Financial management support
  • Digital tool proficiency

Key Requirements

  • Bachelor's degree in scientific or healthcare discipline
  • Minimum of 1 year on-site monitoring experience
  • Proficiency in Microsoft Word, Excel, PowerPoint

Work Rights

Not specified

Tailored Resume

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