Clinical Research Coordinator
About The Position
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.
Requirements
- Experience with EDC platforms and clinical trial data entry required
- Strong understanding of GCP and clinical research workflows
- Excellent organizational, communication, and multitasking skills
- Ability to work independently and collaboratively within a team environment
- Phlebotomy trained and comfortable performing blood draws
Nice To Haves
- 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
- Experience using CRIO CTMS, eSource, and eRegulatory systems preferred
- Familiarity with IRT systems preferred
- Experience maintaining regulatory documentation and essential study files
- CRC certification is a plus but not required
- Medical assistant, nursing, healthcare, or research background preferred
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
Benefits
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
