Oncology Clinical Research Coordinator - 238398 at Medix™ Santa Maria, CA
Behavioral Health Market Context
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Job Description
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: Santa Maria, CA
Pay: $35/hr-$45/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)
• 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: Santa Maria, CA
Pay: $35/hr-$45/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)
Qualifications
- •2+ years as a Clinical Research Coordinator
- •Oncology experience required
- •BLS Certification required
- •Knowledge of clinical research protocols, GCP, and FDA regulations
- •Strong organizational, communication, and multitasking skills
Benefits
- •Pay: $35/hr-$45/hr (Dependent on background and years of experience)
- •Hours: Monday - Friday; Normal Business Hours; Onsite 5 Days a Week
Responsibilities
- •Coordinate and manage clinical trials to ensure compliance with protocols, regulations, and institutional policies, supporting participant safety and study integrity
- •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
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