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: $32.00 per hour
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Medical specialties:
- Hematology
- Oncology
Schedule:
- 8 hour shift
Education:
- Bachelor's (Required)
Experience:
- Clinical Trials: 2 years (Required)
Ability to Relocate:
- Orange, CA: Relocate before starting work (Required)
Work Location: In person