Job Description

Genesis Orthopedics & Sports Medicine is seeking a motivated, organized, and detail-oriented Clinical Research Coordinator to join our growing research department in Oak Brook, Illinois. This is a full-time, on-site position (Monday through Friday, 40 hours per week) with opportunity for long-term growth within a rapidly expanding clinical research program. We are looking for candidates with prior clinical research experience who thrive in a fast-paced environment, can independently manage multiple studies, and are passionate about patient care and advancing clinical research. Responsibilities Coordinate and manage clinical trials from study startup through closeout Independently manage 3 to 4 active studies simultaneously Recruit, screen, consent, and schedule study participants Conduct and support study visits in accordance with protocol requirements Perform accurate source documentation and timely data entry Enter and maintain study data within EDC systems Utilize IRT systems for patient randomization and drug accountability Maintain regulatory binders and essential study documents Assist with IRB submissions, regulatory maintenance, and study updates Communicate with sponsors, CROs, monitors, investigators, and patients Ensure protocol compliance, GCP adherence, and audit readiness Support patient retention and follow-up efforts Assist with lab processing, specimen handling, and shipment preparation as needed Qualifications Minimum 1 to 2 years of clinical research experience preferred Experience working on studies within the musculoskeletal (MSK) and cardiometabolic therapeutic areas preferred Ability to independently manage multiple studies and competing deadlines Phlebotomy trained and comfortable performing blood draws Experience using CRIO CTMS, eSource, and eRegulatory systems preferred Experience with EDC platforms and clinical trial data entry required Familiarity with IRT systems preferred Experience maintaining regulatory documentation and essential study files Strong understanding of GCP and clinical research workflows Excellent organizational, communication, and multitasking skills Ability to work independently and collaboratively within a team environment CRC certification is a plus but not required Medical assistant, nursing, healthcare, or research background preferred Full-time, on-site position Monday through Friday Opportunity for professional growth and advancement Exposure to a variety of therapeutic areas and clinical trials Supportive and collaborative team environment Opportunity to grow within an expanding research program #J-18808-Ljbffr

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