Top 1 Sports scientist Jobs in Chicago Il

Clinical Research Coordinator
Genesis Orthopedics & Sports Medicine —Oak Brook, IL
- Full-time
- Mid-level
- In-person
- Communication skills
- Opportunities for advancement
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Clinical Research Coordinator

Genesis Orthopedics & Sports Medicine -
Oak Brook, IL

Quick Apply

Job Details

Full-time

Benefits

Opportunities for advancement

Qualifications

Filing
Phlebotomy specimen handling
Research project coordination
Clinical data entry
Clinical quality assurance standards
Documentation Handling
Quality data entry
Research compliance audit records management
Research compliance quality assurance records management

Full 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

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

Quick Apply

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