Clinical Trial Associate (On-Site) — Warsaw

ICON San Antonio

Województwo mazowieckie

Presencial

PLN 80 000 - 110 000

Tempo integral

há 6 horas
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Vantagens oferecidas por esta oferta de emprego

Annual leave
Health insurance
Retirement planning
Employee Assistance Programme
Life assurance

Resumo da oferta

ICON Strategic Solutions in Warsaw seeks a Clinical Trial Associate to assist in the design and analysis of clinical trials, interpreting complex medical data and supporting the advancement of therapies. This is a local CTA role based at the client’s Warsaw office, full-time.

You will coordinate trials, manage essential documents, and collaborate with cross-functional teams to ensure proper execution and adherence to regulatory requirements.

Qualificações

  • Bachelor's degree in a scientific or healthcare-related field.
  • At least one year of CTA or Study Coordinator experience.
  • Knowledge of clinical trial processes, regulations and guidelines.
  • Excellent organizational and communication skills.
  • Ability to work full time from Client's office in Warsaw.

Responsabilidades

  • Support the design and analysis of clinical trials and interpret medical data.
  • Coordinate and administer clinical trials ensuring compliance with protocols and regulatory requirements.
  • Maintain trial documentation and regulatory submissions.
  • Collaborate with cross-functional teams to ensure smooth trial execution and track trial metrics.

Conhecimentos

Clinical research
Regulatory knowledge
Organization
Communication

Formação académica

Bachelor's degree in science/healthcare

Descrição da oferta de emprego

ICON Strategic Solutions in Warsaw seeks a Clinical Trial Associate to assist in the design and analysis of clinical trials, interpreting complex medical data and supporting the advancement of therapies. This is a local CTA role based at the client’s Warsaw office, full-time.

You will coordinate trials, manage essential documents, and collaborate with cross-functional teams to ensure proper execution and adherence to regulatory requirements.

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