Research Coordinator

Ophthalmology Ltd • Sioux Falls, SD

387d

About The Position

The Research Coordinator at Ophthalmology LTD plays a crucial role in managing clinical trials and ensuring the well-being of ophthalmic patients. This full-time position requires strong organizational skills and attention to detail, as the coordinator will oversee patient visits, coordinate study-related activities, and ensure compliance with regulatory guidelines. The ideal candidate will work closely with the research team to provide exceptional care and support throughout the clinical trial process.

Requirements

• High School Diploma or equivalent; a college degree or significant relevant experience preferred.
• Minimum of 2 years medical hospital/clinic experience or equivalent with knowledge of medical terminology.
• Prior experience as an Ophthalmic Technician or in research preferred.
• Effective verbal and written communication skills.
• Excellent organizational skills and attention to detail.

Nice To Haves

• Certification as a CCRC, COA, or COT is encouraged.
• Ability to learn quickly and work as a team player.

Responsibilities

• Assists with study initiation activities, including coordinating paperwork and participating in study-initiation meetings.
• Works with Finance Manager to establish budgets, track invoices, and assist in budget reconciliation.
• Oversees patient recruitment, screening, scheduling, and informed consent activities.
• Prepares patient charts for visits and ensures complete data collection.
• Assists clinical research technicians with case report form completion as requested.
• Monitors visits with sponsor staff and prepares regulatory documents.
• Ensures protocol and regulatory compliance for clinical studies.
• Communicates clinical study information with sponsors, investigators, and study participants.
• Manages and maintains all regulatory information about the study.
• Maintains accurate clinical study documentation in accordance with protocols and regulations.
• Tracks study supply inventory and re-orders as necessary.
• Collects, processes, packages, and ships research specimens according to regulations.
• Extracts data from source documents for research studies as directed.
• Collects and reports all Adverse Events and Serious Adverse Events within required timelines.
• Assists with other research and clinical duties as assigned.

Benefits

• Strong compensation and benefit package offered to all employees.

What This Job Offers

• Job Type: Full-time
• Industry: Ambulatory Health Care Services
• Education Level: High school or GED