Research Coordinator (Post-Concussion Study)

The Geneva Foundation•Colorado Springs, CO

12d•$22 - $23•Onsite

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. Must have a flexible schedule. A government background check will be administered. Salary Range $22.00 - $23.00 Hourly. 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 be within a reasonable commute, possibly 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
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

Nice To Haves

2-4 years’ experience in clinical research preferred
2-4 years’ non-profit, research, or healthcare experience desired

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) 0–12 hours, 24 hours, 2 weeks: 2–3 hours each, includes blood draws and clinical testing 1 month, 3 months: 1–2 hours each, involves outcome measures only
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; 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