Clinical Research Coordinator
4 days ago
Vance Thompson Vision Clinic Prof L is a leading provider of vision care services, dedicated to delivering exceptional patient experiences and advancing the field of ophthalmology.
Salary:
$65,000 - $80,000 per year, depending on experience and qualifications.
Job Description:
We are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team. As an Ophthalmic Assistant - Research, you will be responsible for assisting with study initiation activities, overseeing patient recruitment, screening, scheduling, and informed consent activities. You will also serve as the primary patient contact, providing high-quality patient care and promptly addressing patient information needs.
Key Responsibilities:
• Assist with study initiation activities, including coordinating delivery of study-related paperwork, equipment, demos, and supplies.
• Oversee and participate in patient recruitment, screening, scheduling, and informed consent activities.
• Serve as the primary patient contact, counseling patients on visit requirements, study purpose, and study costs, and providing high-quality patient care by promptly addressing patient information needs.
• Prepare patient charts for patient visits, ensuring complete data collection, and assist clinical research technicians with case report form completion as requested.
• Assist in monitoring visits with sponsor staff, including queries, source document reconciliation, preparing regulatory documents, and answering questions.
• Ensure protocol and regulatory compliance to assigned clinical study protocols.
• Serve as the primary liaison between clinical study sponsors, patients, and VTV staff regarding study protocol requirements, and communicate clinical study information with study participants, physicians, clinical study project team, and clinical research manager in an appropriate format.
• Maintain study regulatory file and test article accountability per internal standards.
• Maintain accurate clinical study electronic and hard copy documentation in accordance with clinical study protocols, applicable regulations, and departmental procedures.
• Assist with report preparation and clinical study communications to external agencies (e.g., FDA, IRB) as requested.
• Represent the clinical research department on internal project teams as requested.
Requirements:
• Bachelor's degree in a health-related field.
• Prior experience in academic, pharmaceutical, or medical device clinical trials.
• Working knowledge in research methodology and federal regulations applicable to clinical trials preferred.
Benefits:
Vance Thompson Vision offers a comprehensive benefits package, including competitive compensation, 401(k) with company contributions, education allowance, and wellness program paired with a lifestyle spending account.
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