Clinical Research Coordinator: Data, Trials & Patient Care

Innovo Research; Pinehurst (NC); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Health Insurance

Disability Insurance

Life Insurance

Paid Time Off

Vision Insurance

Job summary

Innovo Research in Pinehurst, NC seeks a Clinical Research Coordinator to manage data and patient records, support investigators, and ensure study procedures align with protocols, SOPs, and GCPs.

The role covers data collection, regulatory submissions, patient recruitment, consent, lab logistics, safety monitoring, and collaboration with physicians, while maintaining confidentiality and quality standards.

Qualifications

• Bachelor's degree in a related field.
• 1-2 years of clinical research experience.
• Experience in a clinical environment or medical setting.
• Proficient in Microsoft Office applications.
• Understanding of medical terminology.
• Working knowledge of clinical trials.
• GCP/ICH and FDA regulations familiarity.
• Knowledge of SOPs, consent forms, and study schedules.
• Phlebotomy and vital signs experience.
• Strong written and verbal communication.
• Integrity and confidentiality.

Responsibilities

• Provide clinical research support to investigators for studies.
• Collect, record, and maintain study data per protocols.
• Submit regulatory/ethics documentation to FDA and others.
• Recruit and screen participants and maintain logs.
• Assist in informed consent and subject orientation.
• Schedule visits and perform study procedures.
• Handle lab testing and logistics.
• Monitor subject safety and report adverse events.
• Prepare for monitoring visits and audits.
• Maintain confidentiality of PHI.

Skills

Microsoft Office

GCP/ICH knowledge

Medical terminology

English communication

Quality control

Time management

Team collaboration

Education

Bachelor's degree in a related field

Job description

Innovo Research in Pinehurst, NC seeks a Clinical Research Coordinator to manage data and patient records, support investigators, and ensure study procedures align with protocols, SOPs, and GCPs.

The role covers data collection, regulatory submissions, patient recruitment, consent, lab logistics, safety monitoring, and collaboration with physicians, while maintaining confidentiality and quality standards.