Clinical Trials Data & Compliance Coordinator

Innovo Research; Hutchinson (KS); On-site; USD 52,000 - 68,000; 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 is seeking a Clinical Research Coordinator to review, process, and manage clinical data and documents in accordance with protocol, SOPs, and GCPs. The role supports investigators in executing studies, coordinating patient enrollment, and maintaining study records in a fast-paced clinical environment.

The CRC will collect and submit regulatory documentation, assist with consent, and participate in daily scheduling, safety monitoring, and data quality checks to ensure high

Qualifications

• Bachelor's degree in a related field.
• 1–2 years of clinical research experience.
• Experience in clinical environments or medical settings preferred.
• Proficient in Microsoft Office applications.
• Understanding of medical terminology and clinical trials.

Responsibilities

• Provide clinical research support to investigators to prepare for and execute studies.
• Collect, record, and maintain study data per protocol and SOPs.
• Recruit and screen participants and maintain screening logs.
• Assist in consent process and orient subjects to the study.
• Maintain source documentation per protocol.
• Schedule and perform study visits and procedures.
• Handle lab testing and specimen logistics.
• Monitor subject safety and report adverse events.

Skills

Attention to detail

Communication skills

MS Office

English proficiency

Education

Bachelor's degree in a related field

Tools

Microsoft Office

Job description

Innovo Research is seeking a Clinical Research Coordinator to review, process, and manage clinical data and documents in accordance with protocol, SOPs, and GCPs. The role supports investigators in executing studies, coordinating patient enrollment, and maintaining study records in a fast-paced clinical environment.

The CRC will collect and submit regulatory documentation, assist with consent, and participate in daily scheduling, safety monitoring, and data quality checks to ensure high