Hybrid Senior CRA – On-Site Monitoring

CTI Clinical Trial and Consulting Services; Covington (KY); Hybrid; USD 65,000 - 100,000; Full time

Benefits offered by this job

Hybrid work-from-home opportunities

Health benefits

Vacation packages

Paid parental leave

Job summary

CTI Clinical Trial and Consulting Services is seeking a Clinical Trial Monitor to manage site activities across phase I–IV studies and Real World Evidence projects. You will perform on-site visits (PSV, SIV, IMV, COV), ensure regulatory compliance, and support start-up, data management, and investigator communications.

You will bring 1 year of on-site monitoring experience and a health-related degree, with hybrid work options and opportunities for professional growth within a global team.

Qualifications

• > At least 1 year of clinical trial monitoring experience or equivalent experience as determined by CTI Management and Human Resources
• > Bachelor's Degree or higher in an allied health field, nursing, pharmacy, or health/science background; RN with an Associate's; or equivalent CTI-defined experience
• > Experience in hospital, pharmaceutical company, or CRO settings with on-site monitoring preferred

Responsibilities

• Serve as the main CTI contact for assigned study sites
• Conduct site visits (PSV, SIV, IMV, COV) and deliverables within Monitoring Plan timelines
• Assist with start-up activities including feasibility and site selection
• Collect, review, and track essential regulatory documents
• Participate in training and meetings for investigators, clients, and project teams
• Create and implement subject enrollment strategies
• Ensure proper storage, dispensation, and accountability of Investigational Product
• Manage site status updates to the Clinical Project Manager
• Conduct remote monitoring per study Monitoring Plan
• Liaise with Clinical Data Management for data cleaning and issue resolution
• Support in contract negotiation with sites and investigator payments

Skills

Clinical trial monitoring

Site management

Regulatory compliance

GCP/ICH familiarity

Communication

Education

Bachelor's degree or higher

RN/health professional background

Nursing diploma or equivalent

Tools

Regulatory documents handling

Job description

CTI Clinical Trial and Consulting Services is seeking a Clinical Trial Monitor to manage site activities across phase I–IV studies and Real World Evidence projects. You will perform on-site visits (PSV, SIV, IMV, COV), ensure regulatory compliance, and support start-up, data management, and investigator communications.

You will bring 1 year of on-site monitoring experience and a health-related degree, with hybrid work options and opportunities for professional growth within a global team.