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
Job Tags
Monday to Friday,