Senior Clinical Trials Operations Coordinator

ThermoFisher Scientific

Roma

Ibrido

EUR 60.000 - 85.000

Tempo pieno

2 giorni fa
Candidati tra i primi
Generatore di candidature

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Descrizione del lavoro

Thermo Fisher Scientific is seeking a Senior Clinical Trial Coordinator to join our global team in supporting over 2,700 trials across 100+ countries. You will coordinate trial activities, ensure regulatory alignment, and train new staff during onboarding.

The role emphasizes process improvements and cross-functional collaboration, with strong emphasis on documentation and system proficiency. You will work with systems such as GoBalto and eTMF, manage study metrics, and support investigator site

Competenze

  • Academic or vocational qualification in life sciences or related field.
  • Bachelor’s degree preferred for higher responsibilities.
  • Minimum 4 years of relevant clinical trial coordination experience.
  • Knowledge of ICH-GCP and regulatory requirements.

Mansioni

  • Coordinate and facilitate project activities for assigned trials.
  • Review and document study files in the appropriate systems.
  • Ensure tasks are completed on time, within budget, and with high quality.
  • Maintain study documentation and provide training to new staff as needed.
  • Support RBM activities and vendor trackers.
  • Prepare and distribute meeting minutes and action items.

Conoscenze

Organizational skills
Attention to detail
Team collaboration
Communication
English proficiency
Time management
Problem solving

Formazione

High/Secondary diploma or equivalent
Bachelor's degree preferred

Strumenti

MS Office
GoBalto
eTMF
Clinical trial databases

Descrizione del lavoro

Thermo Fisher Scientific is seeking a Senior Clinical Trial Coordinator to join our global team in supporting over 2,700 trials across 100+ countries. You will coordinate trial activities, ensure regulatory alignment, and train new staff during onboarding.

The role emphasizes process improvements and cross-functional collaboration, with strong emphasis on documentation and system proficiency. You will work with systems such as GoBalto and eTMF, manage study metrics, and support investigator site

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