Clinical Research Coordinator II — Patient-Focused with Growth Path

ObjectiveHealth; Little Rock (AR); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Competitive compensation

401(k) with Company match

a clear career pathway for advancement

Short- and Long-Term Disability

Health Savings and Flexible Spending 0

Health, Dental and Vision insurance Pl

Generous PTO

Adoption Assistance

Paid Holidays

a wide selection of other voluntary

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator II to manage patient-focused trial activities in a full-time role. The ideal candidate will have 3+ years of clinical research coordination experience and a strong desire to work directly with patients.

The role emphasizes ensuring protocol compliance, patient safety, accurate data entry, and collaboration with the research team to improve enrollment metrics and patient outcomes at participating sites.

Qualifications

• 3+ years of clinical research coordination experience.
• Strong desire to work directly with patients.
• Experience conducting IRB approved clinical trial protocols: identification, screening, randomization, enrollment.

Responsibilities

• Take ownership of assigned studies and patients.
• Communicate promptly with leadership and coworkers when action is needed.
• Maintain punctuality and reliability in daily activities.
• Ensure strict compliance to applicable laws and governing body requirements.
• Learn and use provided technologies to increase efficiency.
• Uphold Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication.

Skills

Patient interaction

Clinical coordination

IRB protocol knowledge

Data entry accuracy

Regulatory compliance

Communication with team

Tools

Esource systems

Job description

ObjectiveHealth is seeking a Clinical Research Coordinator II to manage patient-focused trial activities in a full-time role. The ideal candidate will have 3+ years of clinical research coordination experience and a strong desire to work directly with patients.

The role emphasizes ensuring protocol compliance, patient safety, accurate data entry, and collaboration with the research team to improve enrollment metrics and patient outcomes at participating sites.