Clinical Research Coordinator II (Imaging) - Los Angeles, CA

for section headings. Use

• for any list of duties/requirements/benefits, and

  for prose. We need to decide what goes into each section. About the role: Could be a paragraph summarizing the role: maybe combine first few sentences: "This Clinical Research Coordinator II position offers an opportunity to play a meaningful role in the successful conduct of clinical trials. While the position is not patient-facing in a direct clinical care capacity, it is patient-adjacent and highly involved in the regulatory and operational aspects of clinical research. In this role, you will support key activities across the clinical trial lifecycle, including: ..." But that includes list; maybe better to keep About the role as a short prose paragraph without list, then Responsibilities as list. We must preserve all substantive information; we cannot omit details. So we need to ensure that all details appear somewhere in the output. Let's extract all sentences/bullets: From description: - "This Clinical Research Coordinator II position offers an opportunity to play a meaningful role in the successful conduct of clinical trials." - "While the position is not patient-facing in a direct clinical care capacity, it is patient-adjacent and highly involved in the regulatory and operational aspects of clinical research." - "In this role, you will support key activities across the clinical trial lifecycle, including:" then list: - Screening participants for protocol eligibility - Supporting the informed consent process - Maintaining accurate source documentation related to research visits - Coordinating protocol-defined enrollment activities and timelines - Supporting Adverse Event (AE) and Serious Adverse Event (SAE) documentation and reporting related to participant safety - Helping ensure research activities remain compliant with FDA, OHRP, IRB, sponsor, and protocol requirements - "This is an excellent opportunity for a clinical research professional who enjoys working in a highly regulated environment, managing time-sensitive responsibilities, and contributing to both participant safety and research integrity." - "The CRC II serves as an important partner to investigators, research teams, sponsors, and regulatory stakeholders, helping ensure clinical trials are conducted accurately, responsibly, and in accordance with applicable requirements." - "The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process." - "Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries." - "Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information." - "Presents information at regular research staff meetings." - "May plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying new research opportunities." - "Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB)." - Then "Primary Duties And Responsibilities" list (similar to earlier but more detailed): - Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process. - Schedules patients for research visits and procedures. - In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug. - Maintains accurate source documents related to all research procedures. - Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries. - Schedules and participates in monitoring and auditing activities. - Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings. - Notifies direct supervisor about concerns regarding data quality and study conduct. - Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines. - May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation. - Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA and local Institutional Review Board. - Maintains research practices using Good Clinical Practice (GCP) guidelines. - Maintains strict patient confidentiality according to HIPAA regulations and applicable law. - May coordinate training and education of other personnel. - May participate in centralized activities such as auditing, Standard Operating Procedure development, etc. - May plan and coordinate strategies for increasing patient enrollment, and/or improving clinical research efficiency. - May identify quality and performance improvement opportunities and collaborate with staff in the development of action plans to improve quality. - May identify new research opportunities and present to investigators - Participates in required training and education programs. - Then "Auto req ID 483717BR" (metadata, drop) - "Minimum Education Required High School/GED" - "Qualifications" - "Additional Qualifications/Responsibilities" (repeat of hybrid schedule) - "This role follows a hybrid work schedule, with a minimum requirement of four days onsite per week at our Los Angeles work location." - "Applicants must be able to meet this onsite requirement and, if hired, must reside within a commutable distance of the work location." - "Required High School Diploma/GED" - "2 years of clinical research-related experience" - "Preferred Bachelor’s Degree in Science, Sociology, or a related field" - "Minimum Salary 60028.80" - "Maximum Salary 102044.8" - "Certificates/Security Clearances/Other" - "City* Los Angeles" - "State* California" - "Job_Category Coordinator" - "Job Code Health-Services health-services" - "Affiliate Sponsor Cedars-Sinai" - "Salary Range $60,000-$75,000" We need to avoid duplication. We'll combine similar info. We need to decide sections: - About the role: maybe a paragraph summarizing the role (first few sentences). We'll include the description about opportunity, patient-adjacent, supporting key activities across clinical trial lifecycle (maybe we can keep that as prose, not list). But we need to preserve the list of key activities; those are duties, so better to put them under Responsibilities. Thus About the role could be: "This Clinical Research Coordinator II position offers an opportunity to play a meaningful role in the successful conduct of clinical trials. While the position is not patient-facing in a direct clinical care capacity, it is patient-adjacent and highly involved in the regulatory and operational aspects of clinical research." That's two sentences. - Responsibilities: list all duties (both from earlier list and Primary Duties). We'll combine into a comprehensive list, avoiding duplicates but preserving all substantive info. Need to be careful not to omit any duty. Let's compile a set of duty statements: From first list (support key activities): 1. Screening participants for protocol eligibility 2. Supporting the informed consent process 3. Maintaining accurate source documentation related to research visits 4. Coordinating protocol-defined enrollment activities and timelines 5. Supporting Adverse Event (AE) and Serious Adverse Event (SAE) documentation and reporting related to participant safety 6. Helping ensure research activities remain compliant with FDA, OHRP, IRB, sponsor, and protocol requirements From later paragraph: - The CRC II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. - Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. - Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. - Presents information at regular research staff meetings. - May plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying new research opportunities. - Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). From Primary Duties list: - Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process. - Schedules patients for research visits and procedures. - In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug. - Maintains accurate source documents related to all research procedures. - Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries. - Schedules and participates in monitoring and auditing activities. - Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings. - Notifies direct supervisor about concerns regarding data quality and study conduct. - Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines. - May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation. - Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA and local Institutional Review Board. - Maintains research practices using Good Clinical Practice (GCP