Remote Senior CRA - Oncology/CNS (Poland) Lead-ready

Worldwide Clinical Trials Limited spółka z ograniczoną odpowiedzialnością

Poland

Remote

PLN 90,000 - 130,000

Full time

4 days ago
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Job summary

Worldwide Clinical Trials Limited spółka z ograniczoną odpowiedzialnością is seeking a Senior Clinical Research Associate for a home-based role in Poland. You will lead site qualification, initiation, monitoring, and close-out activities while ensuring GCP, regulatory requirements, and SOPs are followed.

You will monitor patient safety, build strong relationships with investigators, and mentor junior CRAs on global studies when required.

Qualifications

  • MD or Pharmacy degree with CRA experience
  • Four-year degree in medical/biological/health/pharmacy with CRA experience
  • Two-year college curriculum with CRA experience, preferably in nursing/life sciences
  • Oncology experience required; ability to lead CRA activities when appropriate

Responsibilities

  • Lead site qualification, initiation, monitoring and close-out in line with protocols and SOPs.
  • Monitor study quality and patient safety through source data verification, consent reviews, CRF and data query resolution.
  • Build relationships with investigators and site teams, providing protocol guidance and training.
  • Coordinate Lead CRA activities on global studies, reviewing visit reports and mentoring other CRAs.
  • Develop monitoring plans and study tools to support effective study delivery.

Skills

Communication skills
Interpersonal skills
Planning
Organization
Time management
Initiative
Problem-solving
Polish language
English language

Education

MD or Pharmacy degree
Bachelor/4-year degree in life sciences
2-year college in nursing or life sciences

Tools

Microsoft Office
IxRS
EDC systems

Job description

Worldwide Clinical Trials Limited spółka z ograniczoną odpowiedzialnością is seeking a Senior Clinical Research Associate for a home-based role in Poland. You will lead site qualification, initiation, monitoring, and close-out activities while ensuring GCP, regulatory requirements, and SOPs are followed.

You will monitor patient safety, build strong relationships with investigators, and mentor junior CRAs on global studies when required.

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