Coordinating Cra´s Webinar

My Medical Sales Jobs

Site monitoring visits
Protocol and study training
Evaluate study site quality
Perform monitoring and site management work for a variety of protocols, site and therapeutic areas

Job Summary

  • Perform monitoring and site management work for a variety of protocols, site and therapeutic areas.
  • 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

Perform monitoring and site management work for a variety of protocols, site and therapeutic areas.

Skills & Requirements

Must-have

  • Site monitoring visits
  • Protocol and study training
  • Evaluate study site quality
  • Manage study progress
  • Maintain Trial Master File
  • Create site documentation

Nice-to-have

  • Mentor clinical staff
  • Collaborate with study team
  • Effective time management
  • Problem-solving skills

Key Requirements

  • 4-5 years on-site monitoring experience
  • 1 year as a SR CRA
  • Bachelor's Degree in scientific discipline or health care
  • Proficiency in Microsoft Word, Excel, PowerPoint
  • Knowledge of GCP and ICH guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter