Medical Monitor

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Medical Monitor based in Canada.

We are seeking a medically qualified professional to provide clinical and scientific oversight throughout the clinical trial lifecycle, with a strong focus on participant safety, data integrity, and regulatory compliance. In this role, you will work closely with investigators, sponsors, and cross-functional clinical research teams to support the safe and effective execution of clinical studies. You will assess safety events, interpret clinical data, contribute to study design, and help ensure adherence to established protocols and international guidelines. The position combines medical expertise, scientific analysis, and stakeholder collaboration in a global, remote working environment. This is an opportunity to influence clinical research quality, strengthen patient protection, and contribute to the development of healthcare solutions.