Onsite Senior Clinical Research Associate, Sponsor Dedicated

Posted last week

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About the role

  • Senior Clinical Research Associate in Poland monitoring clinical trials and collaborating with leading pharma companies. Offering expertise and career growth in clinical research settings.

Responsibilities

  • 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

  • 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

  • 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

Job title

Senior Clinical Research Associate, Sponsor Dedicated

Job type

Experience level

Senior

Salary

PLN 171,900 - PLN 375,700 per year

Degree requirement

Bachelor's Degree

Location requirements

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