Clinical Research Associate II - Site Monitoring

IQVIA LLC

Lisboa

Presencial

EUR 35 000 - 52 000

Tempo integral

14 dias+
Gerador de candidaturas

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Vantagens oferecidas por esta oferta de emprego

Company car
Mobile phone
Benefits package

Resumo da oferta

IQVIA is seeking a Clinical Research Associate to support site selection, initiation, monitoring and close-out visits across studies. The role involves ensuring regulatory compliance and data integrity while coordinating with study sites and client representatives.

The successful candidate will have a university degree in a scientific field or health care, 2-4 years of independent on-site monitoring experience, and fluent Portuguese and English.

Qualificações

  • University degree in scientific discipline or health care.
  • 2-4 years of independent on-site monitoring experience.
  • Very good computer skills including MS Office.
  • Excellent command of Portuguese and English language.
  • Organizational, time management and problem-solving skills.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  • Flexibility to travel.
  • Driver’s license class B.

Responsabilidades

  • Performing site selection, initiation, monitoring and close-out visits.
  • Supporting the development of a subject recruitment plan.
  • Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and ICH guidelines.
  • Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions.
  • Collaborating with experts at study sites and with client representatives.

Conhecimentos

MS Office
Portuguese
English

Formação académica

University degree in scientific discipline or health care

Descrição da oferta de emprego

IQVIA is seeking a Clinical Research Associate to support site selection, initiation, monitoring and close-out visits across studies. The role involves ensuring regulatory compliance and data integrity while coordinating with study sites and client representatives.

The successful candidate will have a university degree in a scientific field or health care, 2-4 years of independent on-site monitoring experience, and fluent Portuguese and English.

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