Clinical Studies Coordinator

Clinical Study Coordinator

Location:

Madrid, Hibrid

Experience:

4+ years in international clinical trial coordination

mAbxience is a global biopharmaceutical company committed to innovation and excellence in the development and manufacturing of biotechnological medicines. We operate with a strong focus on quality, regulatory compliance, and scientific rigor to improve patient outcomes worldwide.

Oversee and ensure the proper execution and follow-up of clinical trials, managing CROs and vendors to meet timelines, quality standards, and regulatory requirements.
Design and manage clinical trial plans, identifying risks and implementing corrective actions.
Coordinate site and investigator selection, budget management, and vendor contracts.
Supervise clinical trial monitoring, investigational product handling, and patient recruitment strategies.
Support quality management through monitoring reports, deviation handling, and protocol amendments.
Master’s degree is a plus.
Fluent in English and Spanish; additional languages are an asset.
Minimum 4 years’ experience coordinating international clinical trials and managing CROs.
Deep knowledge of international clinical trial regulations (ICH-GCP, FDA, EMA).
Flexible start time from Monday to Friday (full-time).
~&##Permanent contract.
~&##We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test.

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