Experienced Clinical Research Associate - Sponsor Dedicated - Türkiye

IQVIA UK

Istanbul, Türkiye
Site selection and monitoring
Regulatory requirements and guidelines
Tracking submissions and recruitment
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.
  • Company car, mobile phone and attractive benefits package

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
  • regulatory requirements and guidelines
  • tracking submissions and recruitment
  • collaboration with study sites
  • excellent computer skills
  • driver's license class B

Nice-to-have

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

Key Requirements

  • at least 1 year of on-site monitoring experience
  • University degree in scientific discipline
  • Experience in Pharma Industry
  • Excellent command of Turkish and English language
  • Turkey based

Work Rights

Not specified

Tailored Resume

Cover Letter