Independent Clinical Research Coordinator II

Exer Urgent Care; Pasadena (CA); On-site; USD 70,000 - 100,000; Full time

Job summary

Exer Urgent Care seeks a Clinical Research Coordinator II to support site operations across Sherman Oaks and surrounding LA areas. Collaborate with the PI to drive study enrollment, screen patients for eligibility, and manage regulatory start-up activities.

You will collect data, ensure quality, and maintain source documents with strict adherence to GCP. The role requires 2–3 years of SCR experience, familiarity with EMR/CTMS, and strong communication skills.

Qualifications

• Bachelor's degree in health science or related field.
• Minimum 2-3 years of clinical research coordinator experience at an investigational site.
• Certification (e.g. CCRC/SCRA) a plus.
• Phlebotomy certificate preferred.

Responsibilities

• Meet enrollment targets by screening and consent with PI guidance.
• Complete feasibility questionnaires and regulatory start-up packages.
• Recruit and enroll patients per eligibility criteria.
• Collect data during visits and ensure timely entry and QA.
• Maintain regulatory and source documentation per SOPs.

Skills

Regulatory knowledge

GCP familiarity

Data entry

EMR proficiency

CTMS proficiency

Communication

Team coordination

Multitasking

Microsoft Office

Education

Bachelor's degree in health science or related field

2-3 years clinical research coordinator experience

Certification (CRC/SCRA) a plus

High school diploma required

Tools

EMR systems

CTMS

Microsoft Office

Job description

Exer Urgent Care seeks a Clinical Research Coordinator II to support site operations across Sherman Oaks and surrounding LA areas. Collaborate with the PI to drive study enrollment, screen patients for eligibility, and manage regulatory start-up activities.

You will collect data, ensure quality, and maintain source documents with strict adherence to GCP. The role requires 2–3 years of SCR experience, familiarity with EMR/CTMS, and strong communication skills.