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Join our general team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.

Job Description Summary

Job Description

THE MEDICAL MONITOR ROLE

The Medical Monitor is a key clinical expert responsible for ensuring the medical and scientific integrity of clinical trials, overseeing patient safety, and supporting study teams in protocol execution. Reporting to the Vice President of Clinical Operations (EU), the Medical Monitor works closely with sponsors, investigators, and internal clinical teams to ensure the highest ethical, medical, and regulatory standards throughout the clinical trial lifecycle.

The role requires expertise in clinical trial design, medical data interpretation,



and regulatory compliance, with a strong focus on patient safety, risk mitigation, and adherence to study protocols.

Essential Job Functions

Medical Oversight & Patient Safety:

• Provide medical monitoring for clinical trials, ensuring the safety and well-being of study participants.
• Review and assess adverse events (AEs), serious adverse events (SAEs), and suspected unexpected serious adverse reactions (SUSARs), ensuring timely reporting and regulatory compliance.
• Serve as the primary medical contact for clinical sites and investigators, addressing protocol-related questions and safety concerns.

Clinical Trial Conduct & Compliance

• Help ensure study adherence to Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and local regulatory requirements.
• Participate in study start-up activities, including protocol development, investigator meetings, and reg

📌 Medical Monitor (Pacobamba)
🏢 Alira Health
📍 Pacobamba