Patient-Centric Clinical Research Coordinator I

Socket.dev; Akron (OH); On-site; USD 42,000 - 58,000; Full time

Benefits offered by this job

401(k) with company match

Short- and long-term disability

Health, dental and vision insurance

Health Savings Account

Generous PTO

Adoption assistance

Paid holidays

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator I to support IRB-approved trials with direct patient care, data collection, and regulatory compliance. You will coordinate patient visits, consent processes, and routine trial activities while maintaining high-quality data entry and adherence to protocol timelines.

The role emphasizes collaboration with investigators, sponsors, and monitors, ensuring compassionate patient interactions and strict protocol execution across

Qualifications

• Certification such as an MA or phlebotomy, or similar.
• Experience conducting IRB approved clinical trial protocol activities.
• Ability to consent patients, perform physical assessments, blood draws, ECG.
• Attention to data entry, regulatory compliance, site visits, protocol adherence.
• Excellent communication with research team, PIs, Sponsors.

Responsibilities

• Take ownership of assigned studies and patients.
• Communicate promptly with leadership and coworkers when corrections are needed.
• Show up on time, every time.
• Maintain strict regulatory compliance with governing bodies.
• Use provided technologies to increase day-to-day efficiency.
• Uphold Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication.

Skills

Patient interaction

Team collaboration

Clinical trial protocol

Direct patient care

Regulatory compliance

Data entry accuracy

Communication skills

Education

MA certification

Phlebotomy certification

Job description

ObjectiveHealth is seeking a Clinical Research Coordinator I to support IRB-approved trials with direct patient care, data collection, and regulatory compliance. You will coordinate patient visits, consent processes, and routine trial activities while maintaining high-quality data entry and adherence to protocol timelines.

The role emphasizes collaboration with investigators, sponsors, and monitors, ensuring compassionate patient interactions and strict protocol execution across