Patient-Centric Clinical Research Coordinator II

ObjectiveGI, Inc.; Folsom, Northern (CA, KY); Hybrid; USD 65,000 - 90,000; Full time

Benefits offered by this job

401(k) with match

Career pathway

Disability insurance

Health savings account

Health insurance

Dental and vision

Paid time off

Adoption assistance

Paid holidays

Voluntary benefits

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator II to join our team in the US on a full-time basis. The successful candidate will coordinate IRB-approved protocols, screen and enroll patients, obtain consent, and perform clinic visits while maintaining data quality.

You will work with research teams, PIs, sponsors, and monitors to advance gastroenterology, urology, dermatology, and oncology trials, ensuring compliance and patient-focused care across studies.

Qualifications

• 3+ years of clinical research coordination experience.
• Experience with IRB-approved clinical trial protocols.
• Experience in consenting patients, physical assessments, blood draws, ECG.
• Strong data entry accuracy and protocol adherence.

Responsibilities

• Identify, screen, randomize, and enroll patients per protocol.
• Conduct clinic visits and direct patient care activities.
• Maintain eSource material and track AE/SAE events.
• Ensure regulatory compliance and site visits.

Skills

Patient interaction

Team player

Strong communication

Attention to detail

Regulatory compliance

Clinical research coordination

Job description

ObjectiveHealth is seeking a Clinical Research Coordinator II to join our team in the US on a full-time basis. The successful candidate will coordinate IRB-approved protocols, screen and enroll patients, obtain consent, and perform clinic visits while maintaining data quality.

You will work with research teams, PIs, sponsors, and monitors to advance gastroenterology, urology, dermatology, and oncology trials, ensuring compliance and patient-focused care across studies.