Clinical Study Monitor

Senior Medical Monitor - Remote (Anywhere in Europe)

Opportunity Overview Join a Contract Research Organization (CRO) with an established presence in 40+ countries including the US and Europe and Asia-Pacific. The organization is dedicated to advancing clinical research through scientific excellence and operational precision, partnering with biopharmaceutical, medical device, and diagnostic companies across all stages of development from registration studies to post-marketing initiatives.

Their key therapeutic strengths include renal, cardiometabolic, and oncology research areas where they are committed to driving meaningful improvements in global health outcomes. Their success is built on a powerful combination of global reach and deep local expertise. By working closely with communities, they foster trust, enhance patient engagement, and enable diverse and representative study populations. This people-centered approach results in stronger clinical data, accelerated recruitment, and more efficient delivery of therapies to the patients who need them.

About the Role

The Senior Medical Monitor is a pivotal member of the Global Medical Monitoring team, responsible for ensuring patient safety and maintaining the scientific and medical integrity of clinical trials. In this role, you will collaborate with cross-functional colleagues to support high-quality study delivery and adherence to regulatory and ethical standards. This is a fully remote position for candidates based in Europe.

Key Responsibilities Provide ongoing medical oversight for assigned clinical trials, ensuring patient safety and adherence to study protocols. Serve as the primary medical contact for study teams, investigators, and sponsors. Review and assess adverse events, SAEs, and all relevant safety documentation. Contribute to the design and development of study protocols, monitoring plans, and related clinical documents. Participate in investigator meetings, site initiations, and continuous data review activities. Support regulatory submissions with expert medical input. Collaborate with clinical operations, biostatistics, regulatory, and other functional teams to drive successful study outcomes.

About You Medical Doctor (MD) qualification required. At least 5 years of experience as a Medical Monitor, with strong expertise in renal clinical research. Solid understanding of GCP, ICH guidelines, and North American regulatory expectations. Proven experience in safety monitoring, adverse event evaluation, and medical data interpretation.

If you are passionate about advancing global health and contributing to impactful clinical research, we encourage you to apply. The organization is an equal-opportunity employer and welcomes applicants from all backgrounds.