LPN / LVN - General

Cynet Health; Santa Monica (CA); On-site; USD 39,000 - 52,000; Full time

Job summary

Cynet Health is hiring an LPN/LVN for a temporary-to-permanent Clinical Research Coordinator role in Santa Monica. The candidate will coordinate enrollment, study visits, and follow-up care for patients in clinical trials.

The ideal candidate has 5+ years in a clinical research setting managing patients, with Blood Draw Certification and EPIC experience required. BLS/CCRC preferred; Spanish or Korean skills are a plus. This on-site role emphasizes compliance and confidentiality.

Qualifications

• Clinical trial coordination experience is required.
• Minimum 5 years in a clinical research setting managing patients.
• Must have Blood Draw Certification.
• EPIC experience is mandatory.
• Spanish or Korean speaking skills are a plus.

Responsibilities

• Coordinate enrollment, study visits, and follow-up care for patients in multiple clinical trials.
• Serve as primary coordinator for complex protocols or patient populations and manage workload.
• Assist in training new research assistants and CRCs as needed.
• Ensure compliance with laws, regulations, and company policies.
• Maintain confidentiality of organizational and patient information at all times.

Skills

Clinical research coordination

Patient care

Computer skills

Education

Blood Draw Certification

Tools

EPIC

Outlook

MS Teams

Word

Excel

Job description

LPN / LVN - General

Profession: LVN / LPN

Specialty: Administrative

Duration: Temporary to Permanent

Shift: Day

Hours per Shift: 8

Experience: Minimum of 5 years in a clinical research setting managing patients

License: Must have Blood Draw Certification

Certifications: BLS, CCRC (preferred)

Must-Have:

• Must be a certified Medical Assistant, Phlebotomist, LVN, RN, or similar.
• Strong computer skills - Outlook, MS Teams, Word, and Excel.
• Patient-facing clinical trials experience is required.
• Knowledge of neurological conditions is a plus.
• EPIC experience is mandatory.
• Spanish or Korean speaking skills are a plus.
• Commute preferred to be 30 minutes or less due to traffic.

Description:This position is a temporary to permanent Clinical Research Coordinator role.The ideal candidate will have experience coordinating enrollment, study visits, and follow-up care of patients participating in clinical trials.The Clinical Research Coordinator will support investigators during multiple clinical research trials.Responsibilities include acting as the primary coordinator for complex protocols or patient populations and consistently exceeding workload expectations.The candidate will assist in training new research assistants and CRCs as needed.The role demands reporting any suspected or potential violations to laws, regulations, and policies promptly.All transactions must comply with company policies and industry regulations.The candidate should maintain a professional appearance and conduct, with an excellent attendance record.Building rapport and maintaining cooperative relationships with staff and physicians is vital.Confidentiality regarding organizational and patient information at all times is mandatory.The position does not accept device management experience or solely data trials experience.The Clinical Research Coordinator must demonstrate knowledge of compliance and legal requirements relevant to the role.