Clinical Research Coordinator (level dependent on experience

Clinical Research Coordinator (level dependent on experience)

Job Category
:
Clinical Research Center

Requisition Number
: CLINI
001988

• Posted :
  August 20, 2026
• Full-Time
• On-site

Showing 1 location

Clinical Research Center
Cincinnati, OH

Coordinate the conduct of Phase I through Phase IVclinicalresearch studiesin accordance with

Good Clinical Practices(GCPs), International Harmonization Guideline and Standard Operating Procedures(SOPs) beginning withpre-study planning through successful completion of all study visits.

What You'll Do:

• Maintaina good levelofknowledge and understanding of assigned protocols, including all protocol requirements forstudyvisits, obtaining informed consent,study visit schedules, tests, procedures, laboratory information, and drug accountability requirements
• Recruit subject volunteers for studies;
  
  Work with the Recruitment Department with developing study-relatedmaterialsand interview questionnaires
• Create source templates for study documentation, complete case report forms, andother study specific documents seekingassistancefrom Senior Clinical Research Coordinator, Principal Clinical Research Coordinator, Team Leaderor Clinical Site Director, as needed
• Ensure consistency and effective communication duringstudyvisits and assure all procedures are conducted in compliance with the clinical protocol;
  Maintainsubjectsafety, assess feedback fromstudy 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 conductstudyvisits;
  Assure all procedures are conducted in compliance with the clinical protocol andin accordancewithall applicable regulations and in compliance withGCPs
• Interact with Investigators or study sponsors as needed to assure the study participantreceivesappropriate medical evaluation and care when needed
• Interact with the sponsor Clinical Research Associate tofacilitatethe sponsor monitoring and database clean-up process
• Attend sponsor Investigator/Study Coordinator meetings asneeded for assigned protocols
• Conduct clinical research in compliance with all applicable regulations;
  Requestassistanceand technical advice from Senior Clinical Research Coordinator, Principal Clinical Research Coordinator, Team Leader, or Clinical Site Director,as needed
• Actively seeksout development opportunities
• Behave cooperatively and constructively;
  Follow all company policies, state, local,federal, and other applicablelawsand guidelines;
  
  Comply with alljob-specific requirements

What You'll Bring:

• 1+ year of experience as a clinical research coordinator or in a similar position within the medical or mental health field
• Bachelor's degree in life sciences or equivalent combination of related experience and education in the medical or mental health field
• Clinical Research Coordinator Certification (CCRC) is preferred
• Associate or Bachelor's Degree in Nursing is preferred
• Advanced Cardiac Life Support (ACLS) is preferred

• 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.

Equal Opportunity Employer/Veterans/Disabled

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
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For further information, please review the Know Your Rights notice from the Department of Labor.