Clinical Research Coordinator

RDI • Van Nuys, CA

1d

About The Position

RDI is seeking a proactive, organized Clinical Research Coordinator (CRC) to manage clinical trials in compliance with regulatory requirements and ethical standards. The CRC oversees day-to-day clinical study operations and serves as a key contact among study participants, investigators, and internal research teams. The role includes recruiting and screening participants, obtaining informed consent, managing data collection, supporting protocol implementation, and helping ensure trials run smoothly from start to finish.

RDI describes long-term growth through its Operator Studio, where employees can build expertise through hands-on work, coaching, and review of real study problems, learn how the business operates, and earn broader responsibility as their judgment develops.

Requirements

• Bachelor's degree in life sciences, nursing, or a related field.
• 1–3 years of experience in clinical research coordination or a related role.
• Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory standards.
• Strong organizational and time-management skills, with the ability to manage multiple studies simultaneously.
• Strong written and verbal communication skills and the ability to engage effectively with participants and stakeholders.
• Proficiency with electronic data capture systems and clinical trial management software.
• Ability to work independently and collaboratively in a fast-paced research environment.

Nice To Haves

• Relevant certifications, such as CRC or CCRA.

Responsibilities

• Recruit and screen study participants and verify their eligibility in accordance with study protocols.
• Facilitate the informed consent process and ensure participants understand study requirements.
• Coordinate and conduct site visits, including data collection and monitoring compliance with study protocols.
• Maintain accurate and complete study documentation, including source documents and regulatory files.
• Collaborate with Principal Investigators and study sponsors, provide updates, and address issues that arise.
• Prepare for audits and inspections by keeping study records current and compliant.
• Assist with managing study budgets and timelines.
• Support protocol implementation and coordinate day-to-day clinical study operations.

Benefits

• Health care plan including medical, dental, and vision coverage.
• Retirement plan, including 401(k) and IRA.
• Life insurance, including basic, voluntary, and AD&D coverage.
• Paid time off, including vacation, sick leave, and public holidays.
• Long-term growth opportunities through the RDI Operator Studio, including hands-on work, coaching, review of real study problems, and the opportunity to earn broader responsibility.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level