Clinical Research Coordinator: Global Trials & Career Growth

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

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).