Research Coordinator – BLES

• Assist with report generation and project close-out support
• Perform data collection responsibilities as assigned
• Promote safety and confidentiality of research participants at all times
• Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures
• Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures
• Plan, implement and maintain data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data
• Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate to specific study objectives and work scope
• Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives
• Organize and facilitate meetings, conferences, and other events associated with research activities; may perform and/or coordinate outreach activities, as appropriate to research objectives
• Document all correspondence and communication pertinent to the research
• Interact and communicate effectively with Principal Investigator, other site personnel, research participants, The Geneva Foundation, and the funding organization

• Bachelor’s degree or equivalent work experience required
• U.S. Citizenship required
• Research coordination and data collection experience highly desired
• 2-4 years’ experience in clinical research preferred
• 2-4 years’ non-profit, research, or healthcare experience desired
• Demonstrate competence in oral and written communication
• Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
• Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
• Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
• Knowledge of CFR, GCP and ICH guidelines

Demonstrates expertise in research coordination, data collection, and adherence to regulatory guidelines such as OSHA, GCP, and GLP. Proficient in managing research protocols and effectively communicating with diverse stakeholders.

• Research Coordination
• Data Collection
• Clinical Research Experience
• Communication Skills
• Microsoft Office Proficiency

• Data Analysis
• Report Generation
• Project Close-Out Support
• Research Protocol Implementation
• Infection Control Procedures
• Good Clinical Practices
• Good Laboratory Practices
• CFR Knowledge
• ICH Guidelines

• Organizational Skills
• Attention to Detail
• Positive Demeanor
• Flexibility
• Diplomatic Communication

• Occupational Safety and Health Administration
• Non-Profit Research
• Healthcare Experience
• Research Subjects Coordination

• Excel
• Microsoft Office Software