Practicante Universitario Investigación Clínica  Gcto

Imsapharma Com Ar

Colombia
Hybrid
Clinical research process
Regulatory area focus
Process improvement projects
The intern will learn and work in the process of drug research in humans, supporting different roles in the area, which will allow them to have a complete vision of clinical studies, emphasizing the regulatory area

Job Summary

  • The intern will learn and work in the process of drug research in humans, supporting different roles in the area, which will allow them to have a complete vision of clinical studies, emphasizing the regulatory area.
  • Responsibilities include supporting the regulatory process and managing essential documents for clinical studies, participating in follow-up meetings, and contributing to multidisciplinary meetings to identify research centers.
  • This internship will expand your knowledge and complement your scientific and epidemiological training on the operation of clinical drug research, with a focus on the development of a clinical study in Colombia.

Matching Summary

The intern will learn and work in the process of drug research in humans, supporting different roles in the area, which will allow them to have a complete vision of clinical studies, emphasizing the regulatory area.

Skills & Requirements

Must-have

  • Clinical research process
  • Regulatory area focus
  • Process improvement projects
  • Microsoft Office Suite
  • Intermediate English proficiency

Nice-to-have

  • Innovative and experimental company
  • Multidisciplinary team learning
  • Scientific and epidemiological training
  • Contribute with restless thinking

Key Requirements

  • Student of Nursing, Bacteriology, Pharmaceutical Chemistry, Microbiologist, Biomedical Engineering or similar Health careers
  • Proficiency in Office (Word, Excel, PowerPoint)
  • Intermediate English

Work Rights

Not specified

Tailored Resume

Cover Letter