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CRA II/III

MEDSIR

remote, romblon, Philippines Full-time June 13, 2026

Found Description

Overview

We are a Barcelona-based fastest-growing company founded by scientific experts. We are dedicated to the design and management of innovative strategic clinical trials in oncology, from study conception to the publication of study results. Together, we create the best strategies that are both clinically relevant and scientifically meaningful. We strive to improve our knowledge of this complex disease and the vast array of available treatments in a fast-innovative way.

Responsibilities

  • Site Monitoring Support & Training: Conduct pre-study, initiation, routine monitoring, and close-out visits to ensure protocol compliance, ICH-GCP, and regulatory requirements. Provide guidance and training to site staff on recruitment strategies, protocol updates, and data entry practices.
  • Patient Safety & Data Integrity: Oversee patient recruitment and enrollment processes, review source documentation, CRFs/eCRFs, and resolve data discrepancies in coll...

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