Clinical Research

• oversee and administer clinical research studies and associated activities
• assist with the development and management of study budgets
• assist with the review of protocol requirements and assist with the collection of impact statements needed to properly assign costs to each assessment/procedure
• provide feedback on the amount of time necessary for conduct staff to administer assessments and procedures as assigned during the budgeting process
• cooperate as necessary with the Geneva Corporate Manager to ensure that studies remain financially healthy, including but not limited to, the review of monthly budget reports as well as budget forecasts
• assist in project planning, and ensure that pre-established work scope, study protocol and regulatory requirements are followed
• recruit and coordinate research subjects, as appropriate, and serves as principal administrative liaison for the project
• oversee and coordinate the provision of administrative and staff services to investigators; develop and maintain record keeping systems and procedures
• assist with the preparation of presentations for required review and approval processes, to include public affairs office review as applicable

Senior Clinical Research Coordinator

• Executes statistical analyses plans independently
• Collaborates with project team members to implement the study design and statistical analyses plans
• Conducts review of administrative claims, electronic medical records, survey and clinical data
• Develops and implements prediction models for member and provider-based interventions
• Researches and analyzes broadly defined business scenarios, trends, and patterns
• Provides technical/analytical advice to staff
• Compiles results of studies for journal publication

Biostatistician – Health Services Research

• Serve as the primary point of contact for the sponsored genetic testing program, including management of relationships with laboratory partners and coordination of case identification activities
• Use registry data to identify relevant cases that support sponsored genetic testing partnerships and fulfill data access requests from scientific collaborators.
• Manage scientific partnerships, including contracting, data-sharing agreements, and ongoing relationship stewardship.
• Build analytic datasets for scientific partnerships and data access requests, collaborating with internal team members who manage data infrastructure, cleaning, and import tools.
• Contribute to the strategic evaluation of the genetic testing program, including analysis of program performance, partnership value, and potential alternative models to inform future funding and program decisions
• Develop regular scientific publications and accessible research insights to be shared with registry participants and the broader community
• Support the scientific activities of the My Retina Tracker® registry program, including annual review and update of data collection modules in collaboration with registry team members
• Contribute to the development of policies and standard operating procedures, pertaining to data access, data privacy, and protection
• Support annual priority and budget planning alongside the SVP and registry team.
• Perform additional responsibilities as needed to support program success.

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Senior Clinical Research Coordinator

Biostatistician – Health Services Research

Clinical Research Lead, Genetic Testing and Registry