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Clinical Research Associate (part time/freelance)

  • TFS
  • Full time
  • United States
  • 07/04/2021

  • Identify, select, and monitor performance of investigational sites for clinical studies.
  • Ensure studies are carried out according to the study protocol, SOPs, and ICH/GCP regulations and study-specific manuals and procedures.
  • Write, contribute and review of clinical protocols, amendments, informed consent forms, study guides, case report forms, IMP release package and any other clinical research related documents.
  • Track and report on progress of study including site activation, patient enrollment, monitoring visits.
  • Act as Sponsor representative for study sites during study visits
  • Oversee proper training of staff members who are working on the study
  • Responsible for TMF maintenance.
  • Contribution in all other study activities as required

Requirements

  • Education: Degree in Health Sciences, preferably Pharmacy, but also Chemistry, Biology, Biochemistry, Veterinary or similar.
  • Languages: Fluent Spanish and English, knowledge of other languages will be an asset.
  • Experience (years/area): +2 years of experience as a Clinical Research Associate.

About TFS

We believe that a company with ethical and transparent values has a better chance of attracting skilled employees and building long-term relationships.

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