Clinical Research Coordinator

COMPREHENSIVE EYECARE PARTNERS LLC GROUP•Las Vegas, NV

37d•Onsite

About The Position

Comprehensive EyeCare Partners is one of the nation’s largest vision care management service organizations. CompEye consists of 12 separate physician practices with >100 physicians focused on providing best-in-class, full-spectrum practice management and administrative services to its affiliated physicians and practices in support of their mission to deliver clinical excellence. Our Mission: Building the nation’s preeminent eye care services company by partnering with world class physicians to drive superior clinical and surgical outcomes, while optimizing the patient experience. Position Summary The Clinical Research Coordinator assists in the coordination and execution of clinical research studies, ensuring adherence to protocols and regulatory guidelines. Work Hours: Monday-Friday 7:30am-4:30pm

Requirements

Two years’ experience in a customer-facing position preferred.
Minimum one-year experience in a medical office or similar healthcare setting that involved direct patient care.
Proficiency in MS Word, Outlook, and Excel.
Familiarity to proficiency with medical office and electronic medical record software (NextGen and ModMed preferred)
Dedication to a patient-centered approach, delivering exceptional patient care.
High school diploma or general educated degree (GED); some college preferred.
Certification as a Medical Assistant, Phlebotomist preferred.
Equivalent experience will be considered.

Responsibilities

Enlist, maintain, and assure protocol compliance for all patients in clinical trials.
Collaborate with physicians to determine patient eligibility for clinical trials.
Ensure site research quality by practicing compliance with Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP), and applicable regulations.
Coordinate patient care in compliance with protocol requirements, including disbursement of investigational drugs and patient teaching.
Review patients for changes in condition, adverse events, protocol compliance, and response to study drug, thoroughly documenting all findings.
Provide a safe environment for patients, families, and clinical staff, adhering to federal, state, and professional regulatory standards.
Assist the research team in various study activities such as recruitment, screening, study visits, and termination.
Enter study data into the data system such as the Case Report Form per protocol requirements.
Perform assigned work safely, adhering to established departmental safety rules and practices; report any unsafe activities or conditions promptly to the supervisor.