Lead Clinical Research Coordinator

COMPREHENSIVE EYECARE PARTNERS LLC • Austin, TX

2d • Onsite

About The Position

Comprehensive EyeCare Partners is one of the nation’s largest vision care management service organization. CompEye is 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, driving superior clinical and surgical outcomes, while optimizing the patient experience. Position Summary The Lead Clinical Research Coordinator supervises the research team in an administrative and compliance capacity while working directly with some of the best physicians in their fields to develop cutting edge treatments.

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.
• Familiarity to proficiency with medical office and electronic medical record software (NextGen and ModMed preferred).
• Proficiency in MS Word, Outlook, and Excel
• Strong written and verbal communication skills, with the capacity to engage effectively with individuals across all organizational tiers.
• Outstanding customer service aptitude.
• High school diploma or general educated degree (GED); some college preferred.
• Certification as a Medical Assistant, Phlebotomist preferred.
• Equivalent experience will be considered.

Responsibilities

• Under direct supervision of a physician, is responsible for enlisting, maintaining, and assuring protocol compliance for all patients in clinical trials.
• Collaborates with physician in determining eligibility of patients for clinical trials.
• Ensures site research quality by practicing compliance with Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations.
• Coordinates patient care in compliance with protocol requirements.
• May disburse investigation drug and provide patient teaching regarding administration.
• Maintains investigation drug accountability.
• In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings.
• Responsible for accurate and timely data collection, documentation, data entry, and reporting.
• Schedules and participates in monitoring and auditing activities.
• Maintains regulatory documents in accordance with SOPs and applicable regulations
• Provides a safe environment for patients, families, and clinical staff at all times through compliance with all federal, state, and professional regulatory standards as issued through OSHA and the CDC.
• Maintains strict patient confidentiality according to HIPAA regulations and applicable law.

Benefits

• Generous Paid Time Off
• Medical, dental, and vision benefits
• Paid Holidays
• Company-paid life insurance
• 401(k)
• Continuing education and professional development opportunities.
• Supportive and collaborative work environment.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED