Clinical Research Associate

hace 5 días


Buenos Aires, Buenos Aires C.F., Argentina Icon A tiempo completo

The Clinical Research Associate (CRA) is a vital component of our team, responsible for ensuring the integrity and quality of clinical studies at investigative sites or remotely. Key responsibilities include monitoring study progress, verifying participant protection, and maintaining accurate records in accordance with established guidelines.

Main activities:

  • Completes onsite and remote monitoring activities as per ICH-GCP guidelines, applicable regulations, and SOPs.
  • Verifies informed consent procedures and protocol adherence to ensure participant safety.
  • Maintains the integrity of clinical data by ensuring compliance with approved protocols, GCP, and applicable regulations.
  • Writes and submits reports detailing site findings and updates tracking systems.


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