Clinical Research Associate

hace 2 días


Ciudad de México, Ciudad de México PSI CRO A tiempo completo

As a Clinical Research Associate at PSI CRO, you will be responsible for conducting and reporting onsite monitoring visits, as well as being involved in study startup and feasibility research. You will also perform CRF review, source document verification, and query resolution, and be responsible for site communication and management. Additionally, you will be a point of contact for in-house support services and vendors, and communicate with internal project teams regarding study progress. You will also support the regulatory team in preparing documents for study submissions.

Qualifications:

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Independent on-site monitoring experience in Mexico
  • Experience in all types of monitoring visits in Phase II / III
  • Full working proficiency in English and Spanish
  • Proficiency in MS Office applications
  • Ability to plan and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.



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