Remote Clinical Trial Assistant | Spain

Syneos Health, Inc.

Madrid

Híbrido

EUR 26 000 - 38 000

Tempo integral

Há 10 dias
Gerador de candidaturas

Recebe uma resposta deste empregador — um currículo e uma carta de apresentação adaptados exatamente ao que estão a contratar.

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Resumo da oferta

Syneos Health is seeking a Clinical Trial Assistant (CTA)/CTC for sponsor-dedicated work in Madrid with remote capability in Spain. The role supports site management, TMF maintenance, and tracking of essential clinical documents within compliant SOPs.

You will assist Clinical Monitoring, coordinate site communications, manage databases, and help prepare meeting minutes. Requires a High School diploma, 2–3 years experience, fluent English, strong communication, and up to 25% travel.

Qualificações

  • High School diploma or equivalent.
  • 2–3 years of previous CTA/CTC experience.
  • Fluent English is required.
  • Good communication and interpersonal skills.
  • Ability to embrace new technologies and travel up to 25%.

Responsabilidades

  • Perform activities in compliance with Corporate and Clinical Operations SOPs and Work Instructions.
  • Assist Clinical Monitoring with site management and sponsor communications.
  • Create and maintain TMF and project files, including audits.
  • Prepare and maintain site manuals and reference tools.
  • Update clinical tracking information in databases.
  • Track documents for investigator sites and project team.
  • Manage shared mailbox and route site requests appropriately.
  • Coordinate ordering, packing, shipping and tracking of site materials.
  • Attend meetings and prepare accurate minutes and action items.
  • Support collection and disposition of Case Report Forms and queries.
  • Maintain field awareness through required training.

Conhecimentos

Fluent English
Good communication
Interpersonal skills

Formação académica

High School diploma or equivalent

Descrição da oferta de emprego

Syneos Health is seeking a Clinical Trial Assistant (CTA)/CTC for sponsor-dedicated work in Madrid with remote capability in Spain. The role supports site management, TMF maintenance, and tracking of essential clinical documents within compliant SOPs.

You will assist Clinical Monitoring, coordinate site communications, manage databases, and help prepare meeting minutes. Requires a High School diploma, 2–3 years experience, fluent English, strong communication, and up to 25% travel.

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