Clinical Research Coordinator: Drive Trials & Data Quality

Innovo Research; Statesville (NC); On-site; USD 52,000 - 78,000; Full time

Benefits offered by this job

Competitive salary

Health Insurance

Dental Insurance

Disability Insurance

Life Insurance

Paid Time Off

Vision Insurance

Job summary

Innovo Research seeks a Clinical Research Coordinator to review, process, and manage clinical data and regulatory documents, and assist with daily workload planning. You will collect, record, report, and interpret data on patients enrolled in studies according to protocol, SOPs, and GCPs.

Responsibilities include recruiting and screening participants, coordinating visits, handling lab logistics, monitoring safety, and maintaining source documentation to ensure study quality and regulatory

Qualifications

• Bachelor's degree in a related field.
• 1–2 years of clinical research experience.
• Proficient in Microsoft Office applications.
• Understanding of medical terminology and clinical trials.
• Knowledge of GCP/ICH and FDA regulations.

Responsibilities

• Provide clinical research support to investigators to prepare for and execute assigned studies.
• Recruit and screen participants for clinical trials and maintain subject screening logs.
• Coordinate visits and schedule study procedures.
• Handle lab testing, specimen collection, and lab logistics.
• Monitor subject safety and report adverse events to the PI.

Skills

Attention to detail

Strong communication skills

Time management

Problem solving

Team collaboration

GCP/ICH knowledge

Education

Bachelor's degree in a related field

Tools

Microsoft Office

Job description

Innovo Research seeks a Clinical Research Coordinator to review, process, and manage clinical data and regulatory documents, and assist with daily workload planning. You will collect, record, report, and interpret data on patients enrolled in studies according to protocol, SOPs, and GCPs.

Responsibilities include recruiting and screening participants, coordinating visits, handling lab logistics, monitoring safety, and maintaining source documentation to ensure study quality and regulatory