Clinical Research Coordinator

Genesis Orthopedics & Sports Medicine; South Carolina; On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Opportunity for professional growth

Collaborative team environment

Job summary

Genesis Orthopedics & Sports Medicine is looking for a Clinical Research Coordinator to support our research department in Oak Brook, Illinois. This full-time, on-site position involves coordinating clinical trials, managing studies, and ensuring compliance with protocols.

Ideal candidates will have 1-2 years of clinical research experience and be comfortable with EDC platforms. This role offers significant growth opportunities within an expanding research program in a supportive team environment.

Qualifications

• Minimum 1 to 2 years of clinical research experience preferred.
• Ability to independently manage multiple studies and competing deadlines.
• Experience with EDC platforms and clinical trial data entry required.

Responsibilities

• Coordinate and manage clinical trials from study startup through closeout.
• Recruit, screen, consent, and schedule study participants.
• Ensure protocol compliance, GCP adherence, and audit readiness.

Skills

Organizational skills

Communication skills

Multitasking

Independently manage studies

Clinical research experience

Education

Experience with EDC platforms

Phlebotomy training

CRC certification (optional)

Tools

CRIO CTMS

eSource

eRegulatory systems

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