Remote Senior CRA – Oncology/CNS with Lead Potential

Worldwide Clinical Trials

Polska

Remote

PLN 240,000 - 360,000

Full time

40 hours ago
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Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to monitor multicenter studies across Poland from a home-based setting. The role emphasizes patient safety, data integrity, and close collaboration with project teams and investigators.

Ideal candidates have significant CRA experience, strong knowledge of GCP, ICH, and regulatory requirements, plus fluency in Polish and English. Travel is regional with possible occasional international visits.

Qualifications

  • Education and experience: An MD or Pharmacy degree with at least 3 years of CRA experience; a four-year degree in medical, biological, physical, health, pharmacy, or a related science with at least 5 years of CRA experience; or a two-year college curriculum or equivalent education/training, preferably in nursing or life sciences, with at least 7 years of CRA experience.

Responsibilities

  • Lead site qualification, initiation, interim monitoring, management, and close-out activities per protocol and SOPs.
  • Monitor study quality and patient safety through source data verification and safety reviews.
  • Build relationships with investigators and site teams, providing ongoing guidance and training.
  • Ensure regulatory, ethics, and TMF documentation are maintained.
  • Coordinate CRAs as a Lead CRA on global studies when required and mentor staff.

Skills

Polish language fluency
English proficiency
Communication skills
Organizational skills
Leadership ability

Education

MD or Pharmacy degree
4-year degree in medical/biological sciences
2-year college curriculum in nursing or life sciences

Tools

Microsoft Office
IxRS
EDC systems

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to monitor multicenter studies across Poland from a home-based setting. The role emphasizes patient safety, data integrity, and close collaboration with project teams and investigators.

Ideal candidates have significant CRA experience, strong knowledge of GCP, ICH, and regulatory requirements, plus fluency in Polish and English. Travel is regional with possible occasional international visits.

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