The Clinical Research Coordinator I performs activities related to coordination and implementation of research protocols within the Beetham Eye Institute and Eye Research Section (both clinical trial and non-trial research). Responsible for ensuring quality adherence to protocol-specific and general regulatory requirements for translational research and clinical study efforts.  Assists in the development and maintenance of recordkeeping systems as well as procedures to rigorously track, prepare and store patient data for research purposes. Performs a variety of complicated tasks, manages sophisticated equipment data transfers and has a wide degree of creativity and latitude. Assists in administration of studies within BEI and may serve as an administrative liaison for multicenter industry and non-industry studies for the BEI team. Individual is expected to work constructively within the BEI research team and cooperate well with the clinical staff and faculty of the BEI.

As a health care organization, we have the responsibility to do everything in our power to care for and protect our patients, our colleagues and our communities. We require that all staff be vaccinated against influenza (flu) as a condition of employment.

• Plans and coordinates the initiation of research study protocols along with the other members of the BEI clinical research team.
• Creates research applications and informed consent documents for industry-sponsored clinical studies and BEI clinical studies for IRB review/approval.
• Maintains accurate and comprehensive clinical trial records.
• Organize and manages IRB submissions for new and ongoing clinical or translational studies.
• Organize and manages BEI staff trial certifications.
• Assists with patient recruitment/enrollment for clinical research studies to meet desired quotas for participants that fulfill existing eligibility criteria.    
• Creates and maintains organized source documents in a timely and accurate manner including (but not necessarily limited to) study enrollment logs, case report forms, and Committee of Human Studies (CHS) applications. Responds promptly and accurately to Protocol Queries.
• Reports serious adverse events (SAE) in a timely fashion.
• Completes assigned reports including periodic and ad hoc reports, as required by the investigator, administrators, funding agencies, and/or regulatory bodies.
• Prepares for and/or attend audits of any BEI clinical trials.
• Assists the principal investigator with various administrative tasks associated with the day-to-day operations of research studies and projects.
• Serves as liaison for Dana Farber Cancer Institute, Beth Israel Deaconess Hospital and other study collaborators.
• Also serves as BEI Medical Retina Fellowship Coordinator. This includes organizing the application process, interviewing process, and credentialing for incoming fellows.  
• Other duties as assigned.