Coordinate the conduct of Phase I through Phase IV clinical research studies in accordance with Good Clinical Practices (GCPs), International Harmonization Guideline and Standard Operating Procedures (SOPs) beginning with pre-study planning through successful completion of all study visits.

What You'll Do:

• Provide direct patient care consistent with good clinical practices and study protocols.
• Administers investigational medications and performs patient assessments during clinic visits as permitted by protocol and delegated by Principal Investigator.
• Ensure consistency and effective communication during study visits; Assure all procedures are conducted in compliance with the clinical protocol; Maintain subject safety, assess feedback from study participant and refer to investigators or other professionals as needed; If applicable, administer study medications based on state licensure, account for medications used
• Coordinate and conduct study visits and assure all procedures are conducted in compliance with the clinical protocol and in accordance with all applicable regulations and in compliance with (GCPs)
• Interact with Investigators or study sponsors as needed to assure study participant receives appropriate medical evaluation and care when needed
• Interact with sponsor Clinical Research Associate to facilitate the sponsor monitoring and database clean-up process
• Attend sponsor Investigator/Study Coordinator meetings as needed for assigned protocols
• Conduct clinical research in compliance with all applicable regulations; Request assistance and technical advice from Senior Clinical Research Coordinator, Principal Clinical Research Coordinator, Team Leader or Clinical Site Director, as needed

What You'll Bring:

• Excellent communication skills, both verbal and written
• Excellent organizational skills
• Good attention to detail
• Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists
• Proficiency with MSOffice Suite
• Minimal experience as a clinical research coordinator or in a similar position within the medical or mental health field
• Valid RN License in the State of Ohio
• Advanced Cardiac Life Support (ACLS) is preferred

Why CTI?

• Advance Your Career - We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
• Join an Award-Winning and Valued Team - We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
• Make a Lasting Impact - We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

Important NoteIn light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website ( www.ctifacts.com ) or from our verified LinkedIn page.

Please Note

• We will never communicate directly with you via Microsoft Teams Messaging or by text message
• We will never ask for your bank account information at any point during the recruitment process

Equal Opportunity Employer/Veterans/Disabled