Clinical Research Coordinator II - Neurology

Clinical Research Coordinator (CRC)Rocky Mountain Multiple Sclerosis Clinic is seeking an experienced Clinical Research Coordinator (CRC) to help reestablish and grow our clinical research program focused on neurological disease.This is an opportunity for an experienced coordinator who thrives with autonomy, takes ownership of their studies, and wants to play a meaningful role in building a high-quality research program. You'll work closely with physicians, research leadership, sponsors, and patients to coordinate industry-sponsored neurology trials while helping shape the workflows and processes that support the program as it grows.For someone interested in research leadership, this role also offers the opportunity to advance into a Research Supervisor position and lead a team of research coordinators as the program expands.What You'll DoCoordinate assigned clinical trials from study start-up through closeoutServe as a primary point of contact for study participants, sponsors, CROs, and monitorsIdentify and pre-screen potential participants and coordinate screening, enrollment, and study visitsPerform protocol-required procedures within scope and training, including vital signs, ECGs, phlebotomy, specimen processing and shipment, questionnaires, and rating scalesMaintain accurate and timely source documentation, case report forms, and EDC data; resolve queries as neededMaintain regulatory and essential study documentation in accordance with ICH-GCP, sponsor requirements, and applicable regulationsCoordinate site initiation, monitoring, audit, and closeout visitsMaintain close communication with investigators regarding patient status, adverse events, protocol deviations, dose modifications, and other study requirementsParticipate in sponsor meetings, investigator meetings, and required study trainingHelp develop efficient research workflows and processes as the clinical research program growsQualificationsMinimum of 2 years of clinical research coordination experience, preferably with interventional clinical trialsExperience independently coordinating study visits and managing day-to-day study requirementsWorking knowledge of ICH-GCP and clinical research regulationsAuthorization to work in the USExperience with EDC systems, source documentation, regulatory documentation, and sponsor monitoringStrong organizational, prioritization, and problem-solving skills with exceptional attention to detailExcellent written and verbal communication skillsAbility to work independently while collaborating effectively with physicians, patients, sponsors, and research teamsComfortable performing patient-facing study procedures such as phlebotomy and ECGs within appropriate scope and trainingWhy Join UsThis is an opportunity to join at an important stage in the development of our research program. You'll have the ability to take meaningful ownership of your studies, work directly with physicians and research leadership, and help shape how clinical research is integrated into an established outpatient neurology practice.As the program grows, there is an opportunity for this position to advance into research leadership, including supervising and developing a team of research coordinators.What We OfferFull-time, Monday–Friday scheduleSchedule flexibility as needs allowCompetitive compensationGenerous paid time offMedical, dental, and vision insurance401k with Company Match