The Clinical Research Coordinator assists Government directors and PIs in managing clinical research projects
including study enrollment
data collection
budget monitoring
and regulatory compliance. Requires a Bachelor’s degree (Master’s preferred)
2-4 years of experience
strong communication skills
and knowledge of CFR
GCP
and FDA regulations. Duties & Responsibilities: Supports Government directors and Principal Investigators (PIs) in the planning
programming
and execution of clinical research projects and protocols and associated activities. Maintains study records in accordance with protocols
study schedules
participant observations
and provides follow-up documentation to the PI. For human research studies
assists with study enrollment and activities related to the conduct of the study. Coordinates one to several simultaneous projects for the PI/director; confers with investigators on experimental design; provides instruction on various research laboratory techniques
and study participant contact procedures. Organizes research information and manages reporting and data collection. Monitors the research study budget
researches equipment/supply catalogs
and recommends purchase requests for projects/protocols in accordance with the IRB. Documents all regulatory research and administrative actions to ensure study compliance. Prepares and delivers required reports and other research documentation to the PI. Prepares correspondence
builds study files
develops schedules
and creates presentation graphics to support the research study. Utilizes available software systems
including accounts tracking systems
publication submissions
purchase orders
credit card purchases
and preparation of forms for incoming and outgoing funds. May require occasional weekend and evening hours. Minimum Qualification and Experience: Required: B.S. in Biological Sciences or a closely related field; Master's degree highly preferred. 2-4 years minimum experience in clinical research. Demonstrated competence in oral and written communication. Must be organized
attentive to detail
and possess a positive
friendly
and professional demeanor. Proficiency with computer skills
including at least intermediate-level experience with Excel and other Microsoft Office software. Knowledge of CFR
GCP
and ICH guidelines. Must successfully complete CITI training and remain current
with completed GCP training and familiarity with GCP in practice. Demonstrated FDA regulatory experience. Why Join Us? At CICONIX
we are committed to providing high-quality services to support military families. By joining our team
you’ll make a direct impact on the lives of children and families in crisis while working in a supportive
mission-driven environment. We offer flexible remote options
competitive pay
and the opportunity to work on meaningful programs that serve those who protect our country. CICONIX
LLC is an Equal Opportunity Employer
including disability/veterans. We participate in E-Verify.