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Lead cra – São Paulo/SP

liberado em 4 de outubro de 2023

SP | São Paulo
Efetivo (CLT)
Biólogo
Bioquímico
Farmacêutico
Químico

Your responsabilities includes

  • Create, review, and maintain trial essential documents, ensuring completeness and accuracy.
  • Support the preparation and review of clinical trial dossiers for Ethics Committees and Health Authorities, ensuring compliance with regulatory requirements.
  • Drive successful project delivery by actively managing allocated projects, providing guidance to CRAs, and advising on critical study-related issues under the guidance of the Clinical Project Manager.
  • Collaborate with global study team members to facilitate project execution and enhance site experience by overseeing clinical trial budgeting, payments, contracts with investigational sites, investigators, and vendors.
  • Assist the Clinical Project Manager in various clinical trial management tasks, including protocol training, ongoing communication with sites, tracking regulatory submissions, recruitment progress, data management, review of Monitoring Visit Reports, trial supply management, and compliance with study timelines and targets.

Qualifications

  • You hold a Bachelor’s degree Graduation in health-related areas (e.g. Medicine, Pharmacy, Pharmacy-Biochemistry, Biology, Biomedicine, among others).
  • This person is expected to have fluent oral and written English.
  • We expect a candidate with at least 7 years in Clinical Research, including 5 years as monitor.
  • We’ re looking for a candidate who is performance-driven, excels in planning and organization, demonstrates critical thinking and a commitment to continuous improvement, possesses strong relationship and collaboration skills, and exhibits effective leadership capabilities.
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Lead cra – São Paulo/SP

liberado em 4 de outubro de 2023
Contrato
Efetivo (CLT)
Local
São Paulo
Profissões
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