Senior Clinical Trial Manager – Home-Based (Poland)

Syneos Health India Private Limited

United States

A distancia

USD 31.000 - 50.000

Jornada completa

14 días+

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

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Ventajas ofrecidas por este puesto de trabajo

Flexible work hours
Career development

Descripción de la vacante

Syneos Health is seeking a Clinical Trial Manager II to oversee Phase 1 trials with a home-based/remote setup from Poland. You will coordinate cross-functional teams, ensure regulatory compliance, manage budgets and timelines, and drive data integrity across CTMS/EDC systems.

The ideal candidate has 5+ years in trial management, deep knowledge of GCP, and experience liaising with investigators and sponsors in a global setting.

Formación

  • 5+ years of clinically oriented trial management experience.
  • Experience managing Phase 1 studies and multi-site trials.
  • Strong knowledge of ICH-GCP guidelines and regulatory requirements.

Responsabilidades

  • Oversee development, coordination, and execution of Phase 1 clinical trials globally/cross-region.
  • Coordinate with PIs, sponsors, and operational teams to ensure milestones, budgets, and timelines are met.
  • Maintain study tools, dashboards, and systems (CTMS, EDC) and ensure data integrity.
  • Monitor patient safety, protocol compliance, risk management, and quality oversight.
  • Lead risk assessment, site activation, enrollment targets, and database lock timelines.

Conocimientos

Clinical trial management
GCP compliance
Regulatory liaison
Budget & forecasting

Educación

Bachelor's degree in life sciences

Herramientas

CTMS
EDC

Descripción del empleo

Syneos Health is seeking a Clinical Trial Manager II to oversee Phase 1 trials with a home-based/remote setup from Poland. You will coordinate cross-functional teams, ensure regulatory compliance, manage budgets and timelines, and drive data integrity across CTMS/EDC systems.

The ideal candidate has 5+ years in trial management, deep knowledge of GCP, and experience liaising with investigators and sponsors in a global setting.

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