Clinical Research Coordinator

SUMMARY

The Cancer and Blood Specialty Clinic is seeking a dedicated Clinical Research Coordinator capable of traveling between Orange and LA County. The ideal candidate will play a crucial role in facilitating clinical research activities, ensuring compliance with protocols, and supporting the advancement of cancer and blood disorder treatments. This position offers a unique opportunity to contribute to cutting-edge research while providing essential support to our clinic's mission of improving patient outcomes.

ESSENTIAL DUTIES AND REPONSIBILITIES

• Study Coordination: Coordinate and manage all aspects of clinical research studies, ensuring compliance with protocols, regulatory requirements, and ethical standards.
• Participant Recruitment: Recruit and screen potential study participants, explaining the study details, obtaining informed consent, and ensuring eligibility criteria are met.
• Clinical Trial Monitoring: Work with monitors and auditors to facilitate site visits, ensuring that the study is conducted in accordance with protocol, Good Clinical Practice (GCP), and applicable regulations.
• Collaboration with Investigators: Collaborate with principal investigators, physicians, and other healthcare professionals involved in the study. Communicate regularly to address issues and ensure the smooth progress of the research.
• Adverse Event Reporting: Monitor and report adverse events, ensuring timely and accurate reporting to regulatory authorities, sponsors, and other relevant stakeholders.
• Documentation and Record Keeping: Maintain accurate and organized study documentation, including case report forms, source documents, and other study-related records.
• Quality Assurance: Implement quality assurance processes to ensure the integrity of study data and compliance with regulatory standards.
• Communication Skills: Effectively communicate with study participants, investigators, sponsors, and other stakeholders. Provide regular updates on study progress and address inquiries.
• Problem-Solving: Identify and resolve issues or challenges that may arise during the course of the study, working proactively to prevent potential problems.

QUALIFICATIONS

• Bachelor's or advanced degree in a relevant field is preferred but not required.
• Experience in clinical research, and knowledge of regulatory requirements. Strong organizational, communication, and interpersonal skills are essential for success in this role and strongly encouraged.
• Traveling to different locations between our Orange County and LA County clinics is required for this position.

Job Type: Full-time

Pay: $26.00 - $43.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Experience:

• oncology/hematology: 1 year (Preferred)
• clinical trial: 1 year (Preferred)

Location:

• Torrance, CA 90505 (Preferred)

Work Location: In person