Impactful Clinical Research Coordinator II

ObjectiveHealth; Timber Ridge (AR); On-site; USD 60,000 - 76,000; Full time

Benefits offered by this job

401(k) with company match

Disability (short and long-term)

Health insurance

Dental insurance

Vision insurance

Paid time off

Adoption assistance

Paid holidays

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator II to join our on-site team in the United States. The role requires 3+ years of clinical research coordination experience and a passion for direct patient interaction.

You will manage patient screening, enrollment, and clinic visits while ensuring regulatory compliance and accurate data entry. Ideal candidates are detail-oriented team players who can coordinate with investigators, sponsors, monitors, and the research team to meet

Qualifications

• 3+ years in clinical research coordination.
• Experience with IRB-approved protocols and patient enrollment.
• Ability to conduct clinic visits and patient care activities.

Responsibilities

• Identify, screen, randomize, and enroll patients per protocol.
• Conduct clinic visits and perform patient care activities (phlebotomy, ECG as applicable).
• Maintain accurate eSource data and regulatory documentation.
• Coordinate with PIs, sponsors, monitors and research team.

Skills

Patient interaction

Clinical coordination

IRB protocol knowledge

Data entry

Regulatory compliance

Communication

Job description

ObjectiveHealth is seeking a Clinical Research Coordinator II to join our on-site team in the United States. The role requires 3+ years of clinical research coordination experience and a passion for direct patient interaction.

You will manage patient screening, enrollment, and clinic visits while ensuring regulatory compliance and accurate data entry. Ideal candidates are detail-oriented team players who can coordinate with investigators, sponsors, monitors, and the research team to meet