Senior Cra

IQVIA

Buenos Aires, Argentina
Gcp, ich guidelines, and regulatory requirements
Clinical trial management systems (ctms)
Electronic data capture (edc) systems
The Senior Clinical Research Associate (CRA) will play a crucial role in the planning, execution, and management of clinical trials

Job Summary

  • The Senior Clinical Research Associate (CRA) will play a crucial role in the planning, execution, and management of clinical trials.
  • You will need to be comfortable collaborating and communicating with a variety of colleagues and customers.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Matching Summary

The Senior Clinical Research Associate (CRA) will play a crucial role in the planning, execution, and management of clinical trials.

Skills & Requirements

Must-have

  • GCP, ICH guidelines, and regulatory requirements
  • clinical trial management systems (CTMS)
  • electronic data capture (EDC) systems
  • site selection, initiation, monitoring and close-out visits
  • protocol and related study training

Nice-to-have

  • collaborating and communicating with colleagues
  • making an impact in the global research market
  • working to make a real difference in patient health

Key Requirements

  • At least 4 years of on-site monitoring experience
  • Advanced in English
  • Bachelor's degree in a health care or other scientific discipline or educational equivalent

Work Rights

Not specified

Tailored Resume

Cover Letter