Research Coordinator (Post-Concussion Study)

The Geneva Foundation • Colorado Springs, CO

119d

About The Position

The Research Coordinator will provide intermittent support on an as-needed basis for a clinical research study focused on post-concussion assessment and follow-up. This role requires the ability to exercise clinical judgment in determining participant eligibility and autonomy in study execution, serving as a stand-in for the Principal Investigator, when necessary. The position involves flexible scheduling, based on participant availability, with no guaranteed hours. Due to the unpredictable nature of post-concussion assessments, rapid response and proximity to the site are essential. This position will be required to work intermittent hours on-site at the U.S. Air Force Academy in Colorado Springs, CO. A government background check will be administered. Salaries are determined based on several factors including external market data, internal equity, and the candidate's related knowledge, skills, and abilities for the position.

Requirements

• Background in athletic training, physical therapy, exercise science, or related clinical discipline
• Clinical experience required to determine eligibility and conduct study procedures
• Must live within 15-20 miles of USAFA for rapid availability
• Ability to work independently and communicate critical updates to PI in a timely manner
• Bachelor's degree or equivalent work experience required
• 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

Responsibilities

• Conduct participant screening and eligibility assessment in alignment with study inclusion/exclusion criteria
• Serve as primary or secondary coordinator for post-concussion study visits (5 visits over 3 months)
• Perform blood draws and coordinate collection of clinical data per study protocol
• 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
• 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
• Organize and facilitate meetings, conferences, and other events associated with research activities
• Document all correspondence and communication pertinent to the research
• Interact and communicate effectively with Principal Investigator and other site personnel

What This Job Offers

• Industry: Professional, Scientific, and Technical Services
• Education Level: Bachelor's degree