PSenior Medical Monitor - Remote (Anywhere in Europe) /ppbr/ppbOpportunity Overview /b /ppJoin 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. /ppbr/ppTheir key therapeutic strengths include renal, cardiometabolic, and oncology research areas where they are committed to driving meaningful improvements in global health outcomes. /ppTheir 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. /ppbr/ppbAbout the Role /b /ppbr/ppThe 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. /ppbr/ppbKey Responsibilities /b /pulliProvide ongoing medical oversight for assigned clinical trials, ensuring patient safety and adherence to study protocols. /liliServe as the primary medical contact for study teams, investigators, and sponsors. /liliReview and assess adverse events, SAEs, and all relevant safety documentation. /liliContribute to the design and development of study protocols, monitoring plans, and related clinical documents. /liliParticipate in investigator meetings, site initiations, and continuous data review activities. /liliSupport regulatory submissions with expert medical input. /liliCollaborate with clinical operations, biostatistics, regulatory, and other functional teams to drive successful study outcomes. /li /ulpbr/ppbAbout You /b /pulliMedical Doctor (MD) qualification required. /liliAt least 5 years of experience as a Medical Monitor, with strong expertise in renal clinical research. /liliSolid understanding of GCP, ICH guidelines, and North American regulatory expectations. /liliProven experience in safety monitoring, adverse event evaluation, and medical data interpretation. /li /ulpbr/ppIf 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. /p