Clinical Research Associate Sr

Trzdev15

Monitor study delivery
Act as primary site contact
Ensure timely and efficient study completion
The CRA is responsible for the delivery of studies at assigned sites and participates in local study teams

Job Summary

  • The CRA is responsible for the delivery of studies at assigned sites and participates in local study teams.
  • The CRA acts as the primary contact with the study site and is responsible for monitoring study conduct to ensure proper delivery of the study.
  • AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.

Matching Summary

The CRA is responsible for the delivery of studies at assigned sites and participates in local study teams.

Skills & Requirements

Must-have

  • Monitor study delivery
  • Act as primary site contact
  • Ensure timely and efficient study completion
  • Manage site performance
  • Support and advise site staff

Nice-to-have

  • Contribute to investigator selection
  • Participate in national investigator meetings
  • Embrace diversity and equality

Key Requirements

  • 3-5 years experience as Monitor or CRA
  • Availability to travel
  • University degree in Biology, Biochemistry, Pharmacy, Nutrition, Biotechnology or related health fields
  • Clinical research monitoring course (mandatory)
  • Advanced English language skills

Work Rights

Not specified

Tailored Resume

Cover Letter