Clinical Research Coordinator

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Gurnee, IL, US

About Company:

Elevate Clinical Research is a mission-driven organization expanding access to high-quality clinical trials across Texas, Louisiana, Illinois, Maryland, Kansas, South Dakota, Hawaii
, and growing. We exist to bring research closer to the communities that need it most, delivering compassionate patient care, operational excellence, and trustworthy data that advances medicine.

At Elevate, your work has real impact. Every role contributes directly to improving health outcomes and bringing new therapies to life. We hire people who care deeply about patients, believe in doing things the right way, and want to grow with a company that’s expanding nationwide.

What We Value

Patients first in every decision and interaction

Access, equity, and bringing research to underserved communities

High-quality, compliant, reliable study execution

Purpose-driven growth and opportunities for advancement

Supportive teams who communicate, collaborate, and care

Why People Join Us

A mission that matters

Clear, structured onboarding

Leadership that listens and supports

Career growth as we expand into new states

A culture built on integrity, teamwork, and accountability

Join Elevate and help build a patient-centered research network that’s changing what clinical trials can look like for communities across the country.

About the Role:

The Clinical Research Coordinator (CRC) plays a pivotal role in the successful execution and management of clinical trials within healthcare settings. This position is responsible for coordinating all aspects of clinical research studies, ensuring compliance with regulatory requirements and institutional policies. The CRC serves as a liaison between investigators, study sponsors, and participants, facilitating effective communication and smooth study progression. By meticulously managing patient recruitment, data collection, and study documentation, the CRC ensures the integrity and quality of clinical research data.

Ultimately, this role contributes to advancing medical knowledge and improving patient care through the rigorous conduct of clinical research.

Minimum Qualifications:

• Bachelor’s degree in a health-related field such as Nursing, Life Sciences, or Public Health.
• At least 2 years of experience coordinating clinical research studies or trials.
• Comprehensive knowledge of clinical trial processes, regulatory requirements, and ethical standards.
• Familiarity with clinical research documentation, including informed consent forms and case report forms.
• Strong organizational skills and attention to detail to manage multiple study activities simultaneously.

Preferred Qualifications:

• Certification as a Clinical Research Coordinator (e.g., ACRP-CRC or SOCRA).
• Experience working with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Advanced knowledge of FDA regulations and Institutional Review Board (IRB) processes.
• Previous experience in patient recruitment and retention strategies for clinical studies.
• Master’s degree in Clinical Research, Public Health, or a related discipline.

Responsibilities:

• Coordinate and oversee the daily operations of clinical trials, including patient recruitment, informed consent, and scheduling study visits.
• Ensure compliance with all regulatory requirements, institutional policies, and Good Clinical Practice (GCP) guidelines throughout the study lifecycle.
• Maintain accurate and up-to-date regulatory documents, case report forms, and study databases to support data integrity and audit readiness.
• Monitor study progress and patient safety by…