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Clinical Research Associate - IQVIA Biotech Poland

IQVIA

Clinical Research Associate - IQVIA Biotech Poland

full-timePosted: Sep 1, 2026Poland, Warsaw

Job Description

IQVIA Biotech Is Hiring experienced Clinical Research Associates (Central-Northern Poland)Join IQVIA today and make an impact on patients’ outcome!Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.ResponsibilitiesPerforming site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentationSupporting the development of a subject recruitment planEstablishing regular lines of communication plus administering protocol and related study training to assigned sitesEvaluating the quality and integrity of site practices – escalating quality issues as appropriateManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution Qualifications/Requirements: A Bachelor's degree in a health care or other scientific discipline or educational equivalent2 years on-site monitoring experience of clinical trials (ideally in CVRM/Oncology)Written and verbal communication skills including good command of Polish and English languageLocation: central-northern Poland (Warsaw, Poznań, Łódź area)​#weareIQVIA #projectpatientfocus #LI-Remote #CRAIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role, when annualized, is 132.800,00 zł - 280.000,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Locations

  • Poland, Warsaw

Required Qualifications

  • A Bachelor's degree in a health care or other scientific discipline or educational equivalent (degree in a health care or other scientific discipline or educational equivalent)
  • 2 years on-site monitoring experience of clinical trials (ideally in CVRM/Oncology) (experience, 2 years)
  • Written and verbal communication skills including good command of Polish and English language (experience)
  • Location: central-northern Poland (Warsaw, Poznań, Łódź area) (experience)
  • ​#weareIQVIA #projectpatientfocus #LI-Remote #CRA (experience)
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com (experience)
  • IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. (experience)

Responsibilities

  • Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
  • Supporting the development of a subject recruitment plan
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

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