Clinical Research Coordinator II — Patient-Centric Trials

ObjectiveHealth; Folsom (CA); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

401(k) with Company match

Competitive compensation

Disability (short/long-term)

HSA and FSA

Health, Dental and Vision insurance

Generous PTO

Adoption assistance

Paid holidays

Career advancement

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator II in California to directly engage with patients and manage IRB-approved studies. The role focuses on screening, enrollment, and clinic visits, with emphasis on data integrity and regulatory adherence.

The successful candidate will coordinate with the research team to ensure high-quality patient care and study execution. We value teamwork, accountability, and proactive communication while supporting professional growth within a

Qualifications

• 3+ years of clinical research coordination experience.
• Experience conducting IRB-approved protocols: screening, randomization, enrollment, clinic visits.
• Ability to consent patients and perform direct patient care activities.
• Strong data entry accuracy and regulatory compliance across study visits.

Responsibilities

• Take ownership of assigned studies and patients.
• Communicate promptly with leadership and coworkers to address questions or corrections.
• Show up on time and maintain professional conduct.
• Ensure compliance with all applicable laws, regulations, and study requirements.
• Learn and use provided technologies to improve daily workflow.
• Uphold company values: Compassion, Integrity, Collaboration, Innovation, Velocity, Dedication.

Skills

Patient interaction

Clinical research coordination

IRB protocol knowledge

Data entry accuracy

Regulatory compliance

Communication

Attention to detail

Job description

ObjectiveHealth is seeking a Clinical Research Coordinator II in California to directly engage with patients and manage IRB-approved studies. The role focuses on screening, enrollment, and clinic visits, with emphasis on data integrity and regulatory adherence.

The successful candidate will coordinate with the research team to ensure high-quality patient care and study execution. We value teamwork, accountability, and proactive communication while supporting professional growth within a