Job Opportunities API

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  Requirements   • 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  Benefits • 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