Clinical Research Associate 2 - Cfsp

IQVIA

Spain
Site selection and monitoring
Subject recruitment planning
Regulatory compliance
At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization

Job Summary

  • At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.
  • Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines.
  • IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.

Matching Summary

At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.

Skills & Requirements

Must-have

  • site selection and monitoring
  • subject recruitment planning
  • regulatory compliance
  • data query resolution
  • site expert collaboration

Nice-to-have

  • career growth resources
  • flexible work schedules
  • therapeutic knowledge building
  • international reputable company

Key Requirements

  • University degree in scientific discipline
  • Experience in Pharma Industry
  • Experience in Clinical Trials environment
  • Excellent command of Spanish
  • Excellent command of English
  • Driver’s license class B

Work Rights

Not specified

Tailored Resume

Cover Letter