CRN

Medix; Roseville (CA); On-site; USD 85,000 - 105,000; Full time

Job summary

Medix Staffing Solutions, Inc. seeks an experienced Clinical Research Nurse (RN) to support a California-based clinical research program. The ideal candidate holds an active California RN license and has prior clinical research experience.

You will participate in medical record reviews, patient screening, scheduling, data entry, regulatory support, and participant follow-up, while ensuring accuracy and compliance. This is a full-time role with regular daytime hours in California.

Qualifications

• Active California RN license required.
• Prior clinical research experience preferred.
• Strong organizational and documentation abilities.
• Excellent communication and detail-oriented work ethic.

Responsibilities

• Review medical records and patient charts to identify potential study participants.
• Conduct phone screenings and coordinate patient referrals.
• Process media referrals and assist with community outreach and referral physician networking.
• Schedule appointments and provide appointment reminders.
• Retrieve medical records and maintain accurate study documentation.
• Perform data entry and general administrative duties, including filing and preparation.
• Conduct non-invasive screening procedures and administer study medication as required by protocols.
• Support informed consent activities as applicable to study responsibilities.
• Monitor and maintain participant E-Diary compliance.
• Maintain and organize source documents and support storage.
• Provide regulatory support and help with ongoing study documentation and organization.

Skills

CA RN license

Clinical research experience

Organizational skills

Communication skills

Documentation skills

Job description

We are seeking an experienced Clinical Research Nurse (RN) to support clinical research operations for an established research program in California. The ideal candidate will have an active California RN license and previous clinical research experience.

This role will support a variety of clinical research activities, including medical record review, patient screening, appointment coordination, clinical assessments, medication administration, regulatory support, and participant follow-up.

Key Responsibilities

Review medical records and patient charts to identify potential study participants.

Conduct phone screenings and coordinate patient referrals.

Process media referrals and assist with community outreach and referral physician networking.

Schedule appointments and provide appointment reminders.

Retrieve medical records and maintain accurate study documentation.

Perform data entry and general administrative duties, including filing, document organization, and appointment preparation.

Conduct non-invasive screening procedures and administer study medication as required by study protocols.

Support informed consent activities as applicable to study responsibilities.

Monitor and maintain participant E-Diary compliance.

Maintain and organize source documents and support source document storage.

Provide regulatory support and assist with ongoing study documentation and organization.

Required Qualifications

Active Registered Nurse (RN) license in California.

Previous clinical research experience.

Strong organizational, communication, and documentation skills.

Ability to manage multiple responsibilities while maintaining accuracy and attention to detail.

Full-time, 40 hours per week.

Monday-Friday, between 8:00 AM and 5:00 PM.