Clinical Research Coordinator C

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Posted Job Title

Clinical Research Coordinator C

Job Profile Title

Clinical Research Coordinator C

Job Description Summary

This position will be a resource for best practices of managing major clinical trials. The coordinator will provide guidance to both study trials and device trials. The incumbent will be a liaison to departmental interaction such as the investigational team, and sponsor. They will be a resource to other members of the team and will oversee the implementation of new clinical trials. Will review all new trials to help identify the challenges and opportunities discovered. Will problem-solve the challenges to implement a plan of action. Work with the regulatory manager to ensure that submissions to the IRB are completed in a timely manner.

Job Description

• Provide assistance to investigators with ocular examination, coordination of clinical trials, including recruiting new patients, maintaining high retention levels, interviewing participants, gathering medical data, coordinating visits with, interdepartmental units (Oncology, neurology, GYN,) PI/Photographers and laboratory personnel, completing records expeditiously,  
• Interact with governmental regulatory agencies regarding human subject research, completing regulatory submissions to the IRB and monitoring compliance with all institutional regulatory guidelines.
• Maintain patient department research shared drive/BOX regarding study, documentation, enrollment logs and visit summaries.
• Complete study abstract for inter-departmental research  departments  requiring ophthalmology services, determine facilities/equipment are available to complete required visits per the protocol required findings, distribute abstract to requesting department/ ophthalmologist/research team, confirm ICF includes required wording for required ophthalmology exam and testing, schedule appointments including emergency visits as required, track patient visits/procedures, follow-up on SAE and AE findings