Clinical Research Coordinator I

About the Role The Research Coordinator I oversees and administers research studies and related activities. They assist in project planning, ensure adherence to the study protocol and regulatory requirements, and may recruit and coordinate research subjects. They serve as the primary administrative liaison and coordinate administrative and staff services for investigators. What You'll Do

• Promote safety and confidentiality of research participants at all times.
• Adhere to 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, The Geneva Foundation, and the funding organization.
• Comply with all the rules and regulations as applicable to assigned duty station.
• Create and adhere to a data quality and quality assurance plan.
• Assist with interim and annual reports. S/he will be the primary liaison at the data collection site and will be responsible for explaining the project to military personnel associated with the study.
• Demonstrate proficiency in performing basic study related procedures.
• Complete required and applicable research training needed to complete research.
• Maintain and update files of all applicable regulatory documentation for IACUC or IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office. What We're Looking For
• Bachelor's degree or equivalent work experience.
• 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.
• 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. Nice to Have
• Experience with military health system research or DoD-related studies (preferred).
• Experience in nonprofit or government research environment. Compensation & Benefits
• Salary: $60,000 - $70,000 per year.
• Benefits include medical, dental, and vision coverage; Flexible Spending Account; Health Savings Account with employer contribution; coverage for employees and family members including domestic partners.
• Short- and long-term disability, Employee Assistance Program, Life & AD&D insurance, 403b retirement plan with employer match, flexible leave options, and 11 paid holidays.