Job Details

CRA II / Senior CRA

6508
  • £Competitive
  • Poznan, Poland
  • Permanent

Clinical Research Associates (CRAII/Senior CRA) – Remote, Poland

We are seeking Clinical Research Associates at CRA II and Senior CRA levels to join a growing clinical research team within a global biopharmaceutical company (FSP model).

Candidates from across Poland are welcome to apply, with preference for those based in Poznań, Bydgoszcz, Łódź, Wrocław and Szczecin.

The Role

As a CRA, you will be responsible for clinical trial monitoring, ensuring protocol compliance, patient safety, data integrity and ICH-GCP standards. Responsibilities include site qualification, initiation, routine monitoring and close-out visits, source data review, query resolution, documentation and collaboration with investigators and site teams.

This is a remote regional role, with approximately 70% of sites within 250 km of your home and around 8–10 monitoring days per month, combining on-site and remote visits. You may manage up to five protocols.

Requirements

  • BA/BS/BSc in Life Sciences, Healthcare or a related field.
  • At least 1 year of independent monitoring experience preferred for CRA I/II.
  • 3+ years of CRA experience preferred for Senior CRA.
  • Strong knowledge of clinical trials, ICH-GCP and applicable regulations.
  • Fluent Polish and advanced English.
  • Valid driving licence and willingness to travel.
  • Strong organisational, communication and problem-solving skills.
  • Ability to work independently and collaboratively in a remote environment.

Experience in Cardiology, Haematology/Oncology, Inflammation, Metabolic Disorders, Neurology or Rare Diseases is advantageous but not essential.

What We Offer

  • Remote-based working with a regional monitoring model.
  • Structured one-month onboarding programme covering systems, processes, study requirements and monitoring procedures.
  • Ongoing support and development.
  • Competitive salary and the choice of company car or car allowance.
  • Opportunity to work across a range of clinical studies and therapeutic areas.

Preferred availability: Candidates with a one-month notice period are particularly encouraged to apply.

Trish Kelly Principal Consultant in Clinical Data Management & Clinical Research

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