Clinical Research Coordinator (level dependent on experience)

Ctifacts; Cincinnati (OH); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Health benefits

Hybrid work opportunities

Paid time off

Job summary

Ctifacts is seeking a Clinical Research Coordinator for our Cincinnati, OH site. The role encompasses coordinating Phase I–IV studies following GCPs, SOPs, and regulatory standards.

You will manage study visits, consent, data collection, and drug accountability while maintaining patient safety and protocol compliance. The ideal candidate has 1+ year CRC experience and a life sciences degree, with preferred CRC and ACLS certifications.

Qualifications

• 1+ year of experience as a clinical research coordinator or in a similar medical/mental health role.
• Bachelor's degree in life sciences or equivalent combination of related experience and education in the medical or mental health field.
• CCRC certification is preferred.
• Associate or Bachelor's Degree in Nursing is preferred.
• ACLS is preferred.

Responsibilities

• Coordinate the conduct of Phase I through Phase IV clinical research studies in accordance with GCPs, ICH guidelines, and SOPs from pre-study planning to completion of all study visits.
• Maintain knowledge of assigned protocols, study visit requirements, informed consent, visit schedules, tests, procedures, and drug accountability.
• Recruit subjects for studies and work with Recruitment to develop study materials and questionnaires.
• Create source templates, complete case report forms, and assist with study documentation as needed.
• Ensure procedures comply with protocol and regulations; maintain subject safety and address participant feedback; administer medications when licensed.

Skills

Experience as CRC

Education

Bachelor's degree in life sciences

Nursing degree (Associate or Bachelor's)

Clinical Research Coordinator Certification (CCRC)

ACLS certification

Job description

Clinical Research Coordinator (level dependent on experience)

Job Category: Clinical Research Center

Requisition Number: CLINI001988

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

Locations

Showing 1 location

Clinical Research Center
Cincinnati, OH

Description

Coordinate the conduct ofPhase I through Phase IVclinicalresearch studiesin accordance withGood 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,studyvisit schedules, tests, procedures, laboratory information, and drug accountability requirements
• Recruitsubject volunteersfor studies;Work with theRecruitment Department withdeveloping 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, TeamLeaderor Clinical Site Director, as needed
• Ensure consistency and effective communication duringstudyvisits and assure all procedures are conducted in compliance with the clinical protocol; Maintainsubjectsafety, assessfeedback fromstudy participantand 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 medicalevaluation 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, TeamLeader, 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 orBachelor's Degree in Nursing is preferred
• 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.

Equal Opportunity Employer/Veterans/Disabled

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
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