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IQVIA

Senior Clinical Research Associate

IQVIA

. Performing site selection, initiation, monitoring and close-out visits .

Posted 4/8/2026full-timeWarsaw • 🇵🇱 PolandSenior💰 PLN 171,900 - PLN 375,700 per yearWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • 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 (GCP) and International Conference on Harmonization (ICH) guidelines
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
  • Collaborating with experts at study sites and with client representatives

Requirements

What you’ll need
  • University Degree in life science or other scientific discipline or apprenticeship in health care
  • Minimum of 3 years of on-site monitoring experience, alternatively an equivalent combination of education, training and experience
  • Strong experience in monitoring of clinical trials
  • Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment
  • Good command of Polish and English language
  • Flexibility to travel

Benefits

Comp & perks
  • Resources that promote your career growth
  • Leaders that support flexible work schedules
  • Programs to help you build your therapeutic knowledge
  • Dynamic work environments that expose you to new experiences
  • Home-office, company car, and more

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
site selectionmonitoringsubject recruitment plan developmentregulatory submissions trackingcase report form (CRF) completiondata query resolutionclinical trials monitoringGood Clinical Practice (GCP)International Conference on Harmonization (ICH)
Soft Skills
strong written communicationstrong verbal communicationattention to detailability to work in a fast pace environmentflexibility to travel