Cedars-Sinai
Clinical Research Coordinator II, Thoracic (Hybrid)
Cedars-Sinai, California, Missouri, United States, 65018
Clinical Research Coordinator II, Thoracic (Hybrid)
Join to apply for the
Clinical Research Coordinator II, Thoracic (Hybrid)
role at
Cedars-Sinai Clinical Research Coordinator II, Thoracic (Hybrid)
Join to apply for the
Clinical Research Coordinator II, Thoracic (Hybrid)
role at
Cedars-Sinai Job Description
This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area.
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. Job Description
This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area.
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).
Primary Duties And Responsibilities
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.
Qualifications
This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area.
Requirements:
High School Diploma/GED required. Bachelor's Degree Science, Sociology or related degree preferred. 2 years Clinical research related experience required.
#Jobs-Indeed
Req ID
: 8277
Working Title
: Clinical Research Coordinator II, Thoracic (Hybrid)
Department
: Cancer - SOCCI Clinical Research
Business Entity
: Cedars-Sinai Medical Center
Job Category
: Academic / Research
Job Specialty
: Research Studies/ Clin Trial
Overtime Status
: EXEMPT
Primary Shift
: Day
Shift Duration
: 8 hour
Base Pay
: $28.30 - $48.11 Seniority level
Seniority level Not Applicable Employment type
Employment type Full-time Job function
Job function Research, Analyst, and Information Technology Industries Hospitals and Health Care, IT Services and IT Consulting, and Research Services Referrals increase your chances of interviewing at Cedars-Sinai by 2x Sign in to set job alerts for “Clinical Research Coordinator” roles.
San Francisco Bay Area $60.00-$70.00 2 weeks ago San Francisco Bay Area $60,000.00-$90,000.00 1 month ago South San Francisco, CA $85.00-$105.00 4 days ago Clinical Trial Assistant I, Clinical Operations
Clinical Research Assistant / Clinical Research / Full-time / Days
Los Angeles, CA $38,272.00-$65,062.00 2 weeks ago Clinical Trial Assistant I, Clinical Operations
San Mateo County, CA $40.00-$45.00 3 weeks ago Clinical Trial Assistant I, Clinical Operations
Beverly Hills, CA $19.50-$32.86 5 days ago Irvine, CA $73,500.00-$92,000.00 4 days ago Foster City, CA $106,000.00-$123,000.00 2 days ago Newport Beach, CA $25.00-$35.00 1 week ago Clinical Research Assistant I - Exercise Oncology
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) (LA)
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr
Join to apply for the
Clinical Research Coordinator II, Thoracic (Hybrid)
role at
Cedars-Sinai Clinical Research Coordinator II, Thoracic (Hybrid)
Join to apply for the
Clinical Research Coordinator II, Thoracic (Hybrid)
role at
Cedars-Sinai Job Description
This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area.
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. Job Description
This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area.
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).
Primary Duties And Responsibilities
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.
Qualifications
This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area.
Requirements:
High School Diploma/GED required. Bachelor's Degree Science, Sociology or related degree preferred. 2 years Clinical research related experience required.
#Jobs-Indeed
Req ID
: 8277
Working Title
: Clinical Research Coordinator II, Thoracic (Hybrid)
Department
: Cancer - SOCCI Clinical Research
Business Entity
: Cedars-Sinai Medical Center
Job Category
: Academic / Research
Job Specialty
: Research Studies/ Clin Trial
Overtime Status
: EXEMPT
Primary Shift
: Day
Shift Duration
: 8 hour
Base Pay
: $28.30 - $48.11 Seniority level
Seniority level Not Applicable Employment type
Employment type Full-time Job function
Job function Research, Analyst, and Information Technology Industries Hospitals and Health Care, IT Services and IT Consulting, and Research Services Referrals increase your chances of interviewing at Cedars-Sinai by 2x Sign in to set job alerts for “Clinical Research Coordinator” roles.
San Francisco Bay Area $60.00-$70.00 2 weeks ago San Francisco Bay Area $60,000.00-$90,000.00 1 month ago South San Francisco, CA $85.00-$105.00 4 days ago Clinical Trial Assistant I, Clinical Operations
Clinical Research Assistant / Clinical Research / Full-time / Days
Los Angeles, CA $38,272.00-$65,062.00 2 weeks ago Clinical Trial Assistant I, Clinical Operations
San Mateo County, CA $40.00-$45.00 3 weeks ago Clinical Trial Assistant I, Clinical Operations
Beverly Hills, CA $19.50-$32.86 5 days ago Irvine, CA $73,500.00-$92,000.00 4 days ago Foster City, CA $106,000.00-$123,000.00 2 days ago Newport Beach, CA $25.00-$35.00 1 week ago Clinical Research Assistant I - Exercise Oncology
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) (LA)
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr