Job Description

Job Summary:

Coordinate and manage clinical trials to ensure compliance with protocols, regulations, and institutional policies, supporting participant safety and study integrity.

Key Responsibilities:

• Facilitate site initiation and sponsor-required training for clinical protocols.
• Dispense study medications and coordinate with pharmacy staff as needed.
• Process and ship lab specimens in compliance with federal regulations.
• Conduct informed consent processes, ensuring proper documentation and compliance.
• Schedule and oversee study visits, tests, and procedures per protocol requirements.
• Accurately collect and report data, maintaining research subject charts and source documents.
• Perform or coordinate clinical procedures (e.g., blood draws, ECGs) with appropriate training.
• Report adverse events, protocol deviations, and violations to study sponsors and IRBs.
• Prepare and submit regulatory documents, including IRB applications and consent forms.
• Support participant recruitment, screening, enrollment, and retention.
• Serve as a liaison between participants, investigators, sponsors, and regulatory bodies.
• Assist in sponsor monitoring visits and audits, resolving findings promptly.

Qualifications:

• 2+ years as a Clinical Research Coordinator
• Oncology experience required
• BLS Certification required
• Phlebotomy Certification preferred
• Knowledge of clinical research protocols, GCP, and FDA regulations.
• Strong organizational, communication, and multitasking skills.
• Experience with clinical procedures and data management preferred.

Details:

Location: Sacramento, CA

Pay: $35/hr-$50/hr (Dependent on background and years of experience)

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

Duration: Contract to Hire (1040 Hours)

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