Senior Remote CTA, Poland — Grow in Global Trials

Parexel

Pol

Híbrido

EUR 25.000 - 27.000

Jornada completa

Hace 4 días
Sé de los primeros/as/es en solicitar esta vacante
Generador de candidaturas

Transforma esta oferta en una entrevista — un currículum y una carta de presentación creados pensando en lo que quiere el empleador.

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Ventajas ofrecidas por este puesto de trabajo

Premium salary
Attractive benefits
Health, Dental & Vision plan
Life insurance
Excellent work environment
Team collaboration
Innovative technology
Excellent training

Descripción de la vacante

Parexel is hiring a Senior Clinical Trial Associate (CTA) for a home-based role in Poland. You will support global study teams across start-up, conduct, and close-out, ensuring adherence to ICH/GCP and regulatory standards.

Key activities include coordinating meetings, maintaining study trackers, and assisting with protocol feasibility and country/site selection. Strong IT skills and language ability are required.

Formación

  • 3+ years of global trial support or project specialist experience.
  • Strong computer skills with CTMS, EDMS and MS-Office suite.
  • Fluent English and Polish, written and spoken.

Responsabilidades

  • Provide logistical support to global study teams across phases.
  • Coordinate study meetings and develop presentation materials.
  • Track study data and maintain CTMS/TMF documentation.
  • Support HA/IRB submissions and regulatory processes.
  • Mentor junior staff and share best practices.

Conocimientos

CTMS
EDMS
MS Office
Excel
Word
Communication
Project management
Regulatory compliance
Language: English
Polish language

Educación

High school diploma
Life science degree preferred
Relevant qualifications

Herramientas

CTMS
EDMS
MS Office

Descripción del empleo

Parexel is hiring a Senior Clinical Trial Associate (CTA) for a home-based role in Poland. You will support global study teams across start-up, conduct, and close-out, ensuring adherence to ICH/GCP and regulatory standards.

Key activities include coordinating meetings, maintaining study trackers, and assisting with protocol feasibility and country/site selection. Strong IT skills and language ability are required.

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