Sr. Cra 2

Ivivamedical

Not specified
Perform site monitoring visits
Administer protocol and study training
Evaluate study site quality and integrity
Ivivamedical is seeking a Sr. CRA 2 to perform monitoring and site management for clinical trials, ensuring compliance with regulatory requirements and effective communication with study sites. The ideal candidate will have at least three years of onsite monitoring experience and a strong understanding of clinical research regulations

Job Summary

  • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
  • Act as a mentor for clinical staff including conducting co-monitoring and training visits.

Matching Summary

Match Score: 85

Ivivamedical is seeking a Sr. CRA 2 to perform monitoring and site management for clinical trials, ensuring compliance with regulatory requirements and effective communication with study sites. The ideal candidate will have at least three years of onsite monitoring experience and a strong understanding of clinical research regulations.

Skills & Requirements

Must-have

  • Perform site monitoring visits
  • Administer protocol and study training
  • Evaluate study site quality and integrity
  • Manage study progress and documentation
  • Maintain Investigator's Site File

Nice-to-have

  • Collaborate with study team members
  • Support development of recruitment plan
  • Effective time and financial management

Key Requirements

  • At least 3 years of on-site monitoring experience
  • Bachelor's Degree in scientific discipline or health care preferred
  • In depth knowledge of GCP and ICH guidelines
  • Proficiency in Microsoft Word, Excel and PowerPoint

Work Rights

Not specified

Tailored Resume

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