Job Description

Summary Of Responsibilities

The research coordinator is primarily responsible for coordinating research patient visits according to both the ICH-GCP guidelines and the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.

Key Responsibilities:

• Coordinate and oversee clinical trials, ensuring adherence to protocols, timelines, and regulatory requirements.
• Recruit, screen, and enroll study participants while maintaining detailed and accurate records.
• Obtain informed consent and ensure participants’ rights and safety are upheld throughout the study.
• Collect, process, and manage study data in compliance with Good Clinical Practice (GCP) guidelines.
• Communicate effectively with investigators, sponsors, and regulatory agencies.
• Prepare and submit study documentation, including IRB submissions and study updates.
• Monitor inventory of study supplies and ensure proper handling of investigational products.
• Conduct regular audits to ensure compliance with study protocols and regulations.

Requirements:

• Bachelor's/Associate's degree required
• 2+ years of experience in Clinical Research
• Experience in Nephrology is a plus
• Phlebotomy/ECG experience required

Details:

Location: Fremont, CA

Pay: $60k-$70k annually (Dependent on background and years of experience)

Hours: Monday - Friday; Normal Business Hours; Onsite 5 Days a Week

Duration: Direct Hire

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