Clinical Research Coordinator: Advance in Phase I–IV Trials

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

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.