Clinical Research Coord II
2 months ago
As a Clinical Research Coordinator II, you willworkindependently 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. You will be responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Will also be 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. You may plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying new research opportunities. Will ensurecompliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).
ESSENTIAL JOB 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.Scheduling of 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 involve 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 investigatorsParticipates in required training and education programs
Qualifications
Educational Requirements:
Bachelor of Arts orBachelor of Science Degree is strongly preferred
Licenses:
ACRP/SoCRA (or equivalent) certification preferred
Experience:
Two (2) years minimum of directly related experience
About Us
Cedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine and research. Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching and community service. Today, Cedars- Sinai is known for its national leadership in transforming healthcare for the benefit of patients. Cedars-Sinai impacts the future of healthcare by developing new approaches to treatment and educating tomorrow's health professionals. Additionally, Cedars-Sinai demonstrates a commitment to the community through programs that improve the health of its most vulnerable residents.
About the Team
Cedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other healthcare professionals and staff. Choose this if you want to work in a fast-paced environment that offers the highest level of care to people in the Los Angeles that need our care the most.
Req ID : HRC0824907
Working Title : Clinical Research Coord II - Smidt Heart Institute - Makkar Lab
Department : Heart Institute
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
-
Clinical Research Coord II
2 months ago
Los Angeles, California, United States Cedars-Sinai Full timeJob DescriptionAs a Clinical Research Coordinator II, you willworkindependently 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. You will be responsible for accurate and timely source documents, data...
-
Clinical Research Coord II
3 days ago
Los Angeles, California, United States Cedars-Sinai Full timeJob DescriptionAs a Clinical Research Coordinator II, you willworkindependently 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. You will be responsible for accurate and timely source documents, data...
-
Clinical Research Coord I
2 months ago
Los Angeles, California, United States Cedars-Sinai Full timeJob DescriptionAs a Clinical Research Coordinator I, you willworkindependently providing study coordination including screening of potential research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. You will be responsible for accurate and timely source documents,...
-
Clinical Research Coord I
3 days ago
Los Angeles, California, United States Cedars-Sinai Full timeJob DescriptionAs a Clinical Research Coordinator I, you willworkindependently providing study coordination including screening of potential research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. You will be responsible for accurate and timely source documents,...
-
Clinical Research Coord I
2 months ago
Los Angeles, California, United States Cedars-Sinai Full timeJob DescriptionAs a Clinical Research Coordinator I, you willworkindependently providing study coordination including screening of potential research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. You will be responsible for accurate and timely source documents,...
-
Clinical Research Coord I
3 days ago
Los Angeles, California, United States Cedars-Sinai Full timeJob DescriptionAs a Clinical Research Coordinator I, you willworkindependently providing study coordination including screening of potential research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. You will be responsible for accurate and timely source documents,...
-
Clinical Research Coord I
2 weeks ago
Los Angeles, California, United States Cedars-Sinai Full timeJob DescriptionThe Clinical Research Coordinator I works independently providing study coordination, 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...
-
Clinical Research Coord I
3 days ago
Los Angeles, California, United States Cedars-Sinai Full timeJob DescriptionThe Clinical Research Coordinator I works independently providing study coordination, 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...
-
Clinical Research Coordinator
1 week ago
Los Angeles, United States Matrix Clinical Research Full timeJob DescriptionJob DescriptionBenefits:401(k)Competitive salaryHealth insurancePaid time offTraining & developmentJob SummaryMust have 3 consecutive years recent experience in a trial studyResponsibilities Provide clinical research support to investigators to prepare for and execute assigned research studies, including: Review study protocols, Case Report...
-
Clinical Research Coord I
2 weeks ago
Los Angeles, United States CEDARS-SINAI Full timeThe Clinical Research Coordinator I works independently providing study coordination, 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...
-
Clinical Research Coord Iii
1 month ago
Los Angeles, United States Springer Nature Full time**Clinical Research Coord III -Cheng Lab, Heart Institute**: - Employer- Cedars-Sinai- Location- Los Angeles, California- Salary- Competitive- Closing date- 1 Jul 2024- Discipline Health Science Job Type Researcher Employment - Hours Full time Duration Permanent Qualification PhD Sector Hospital- You need to sign in or create an account to a...
-
Clinical Research Coord Iii
1 month ago
Los Angeles, United States CEDARS-SINAI Full timeThe Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and specialized care teams treat the full spectrum of heart...
-
Clinical Research Coord III
2 weeks ago
Los Angeles, United States Cedars-Sinai Full timeJob Description The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and specialized care teams treat the full...
-
Clinical Research Associate II
1 month ago
Los Angeles, California, United States Cedars-Sinai Full timeJob DescriptionWe invite you to consider this great opportunityWhen the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai.Dr. Omar Al-Louzi, MD is seeking a highly motivated Clinical Research...
-
Clinical Research Associate II
3 days ago
Los Angeles, California, United States Cedars-Sinai Full timeJob DescriptionWe invite you to consider this great opportunityWhen the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai.Dr. Omar Al-Louzi, MD is seeking a highly motivated Clinical Research...
-
Clinical Research Coord I
2 weeks ago
Los Angeles, United States Cedars-Sinai Full timeJob DescriptionThe Clinical Research Coordinator I works independently providing study coordination, 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...
-
Clinical Research Coord I
2 days ago
Los Angeles, United States Cedars-Sinai Full timeJob DescriptionThe Clinical Research Coordinator I works independently providing study coordination, 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...
-
Clinical Research Coord III
1 month ago
Los Angeles, United States Cedars-Sinai Full timeJob DescriptionThe Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and specialized care teams treat the full...
-
Clinical Research Coord III
2 days ago
Los Angeles, United States Cedars-Sinai Full timeJob DescriptionThe Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and specialized care teams treat the full...
-
Research Coordinator
2 weeks ago
Los Angeles, United States Matrix Clinical Research Full timeJob DescriptionJob DescriptionJob SummaryMust have 3 consecutive years recent experience in a trial studyResponsibilities · Provide clinical research support to investigators to prepare for and execute assigned research studies, including:· Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems...