General Activities: Manages clinical investigational sites. Trains and provides direction to the investigators and the staff of the sites. Reviews, verifies and ensures that clinical documentation fulfils all protocol, GCP and regulatory requirements and maintains drug accountability.
MMATISS offers a wide range of professional development opportunities. If you are an outstanding professional and you’re interested in joining our team, do not hesitate to send your resume to the address described below.
Contact MMATISS:
[email protected]
📌 Clinical Research Associate CRA (México)
🏢 Mmatiss
📍 México