Clinical Research Coordinator (level dependent on experience)

CTI; Cincinnati (OH); Hybrid; USD 52,000 - 68,000; Full time

Benefits offered by this job

Health benefits

Hybrid work opportunities

Paid parental leave

Job summary

CTI Clinical Trial and Consulting Services is seeking a Clinical Research Coordinator to support Phase I–IV studies, ensuring protocol adherence, patient safety, and accurate documentation. The role involves coordinating study visits, assisting with source templates, and collaborating with investigators and sponsors to maintain high-quality data and participant care.

The ideal candidate has 1+ year of clinical research experience, a life sciences degree, and relevant certifications (CCRC, ACLS).

Qualifications

• 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.

Responsibilities

• Maintain good knowledge and understanding of assigned protocols and visit requirements.
• Recruit subjects for studies and collaborate with Recruitment Department on materials and interview questions.
• Create source templates, complete case report forms, and other documents with guidance as needed.
• Ensure study procedures are conducted per protocol, maintain subject safety, and assess participant feedback.
• Coordinate and conduct study visits and ensure compliance with regulations and GCPs.
• Interact with Investigators, sponsor monitors, and study staff to ensure participant care and data integrity.
• Attend sponsor Investigator/Study Coordinator meetings as assigned.

Skills

Clinical research experience

Education

Bachelor’s degree in life sciences

CCRC certification

Nursing degree (Associate or Bachelor’s)

ACLS certification

Job description

About CTI

CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com

Coordinate the conduct of Phase 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 withdevelopingstudy-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’sdegree in life sciences or equivalent combination of related experience and education in the medical or mental health field
• Clinical Research Coordinator Certification (CCRC) ispreferred
• Associate orBachelor’s Degree in Nursing is preferred
• Advanced Cardiac Life Support (ACLS) ispreferred

Why CTI?

• Advance Your Career – We invest in your professional growth. Through a structured mentoring program, leadership development courses, and access to ongoing education and training opportunities, including tuition reimbursement, you’ll have the tools to achieve your goals. Our dedicated training department supports your successful career at CTI.
• Be Part of an Award-Winning Team – Join a global team spanning 60 countries, recognized for its award-winning culture that prioritizes people. We support your work-life balance with generous health benefits, vacation packages, hybrid work opportunities, and paid parental leave. Through our CTI Cares program, you’ll have opportunities to give back to your community and the world.
• Make a Lasting Impact – At CTI, your work directly contributes to advancing medicine. You’ll play a vital role in developing life-changing treatments for patients with chronic and critical illnesses. Together, we move medicine forward, making a difference for those who need it most.

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