Medical Monitor – Rheumatology (Canada/Argentina)

About the role

The Medical Monitor, Rheumatology, provides medical and scientific oversight for clinical research programs in rheumatology. You will ensure data integrity, subject safety, and timely communication with investigators, sites, and internal teams.

Key responsibilities

• Stay current on study protocols, amendments, Investigator’s Brochure, and safety information.
• Develop and review the Medical Monitoring plan and deliver protocol‑related training.
• Participate in investigators’ meetings and safety review meetings.
• Provide 24/7 on‑call support for urgent safety matters, including emergency unblinding.
• Advise sites on protocol inclusion/exclusion criteria, concomitant medications, and eligibility issues.
• Review laboratory critical values, assess prohibited medication impact, and recommend appropriate actions.
• Support dropout subject replacement decisions and overall medical advisory functions.

Required profile

• Proven ability to build positive relationships with clinical sites, sponsors, and internal stakeholders.
• Strong understanding of clinical research protocols and the practical realities of trial execution.
• Capacity to interpret large volumes of data quickly and provide clear medical guidance.

Required skills