Clinical Research Coordinator I
3 months ago
Come join our team
The 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 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 study information at regular research staff meetings. 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.
- Participates in required training and education programs.
Qualifications
Educational Requirements:
- High School Diploma/GED required
- Bachelor's Degree in Science, Sociology or related degree preferred
Licenses:
- SOCRA or ACRP Certification preferred upon hire
Experience:
- One (1) year of clinical research related experience required
About UsCedars-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 TeamCedars-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 : 4391
Working Title : Clinical Research Coordinator I - Obstetrics & Gynecology - Maternal-Fetal Medicine (Part-Time, Hybrid)
Department : Research - OBGYN
Business Entity : Cedars-Sinai Medical Center
Job Category : Academic / Research
Job Specialty : Research Studies/ Clin Trial
Overtime Status : NONEXEMPT
Primary Shift : Day
Shift Duration : 8 hour
Base Pay : $23.39 - $39.76
-
Clinical Research Coordinator I
3 weeks ago
Modesto, California, United States CEDARS-SINAI Full timeJob DescriptionThe Clinical Research Coordinator I at CEDARS-SINAI plays a crucial role in the success of our research studies. This position is responsible for providing study coordination, screening potential patients for protocol eligibility, and presenting non-medical trial concepts and details. The Clinical Research Coordinator I will also participate...
-
Clinical Research Coordinator I
4 weeks ago
Modesto, California, United States Cedars-Sinai Full timeJob OverviewCedars-Sinai is seeking a highly skilled Clinical Research Coordinator I to join our team. The successful candidate will be responsible for providing study coordination, screening potential patients for protocol eligibility, and presenting non-medical trial concepts and details.Coordinate clinical research studies, including screening patients...
-
Clinical Research Associate I
4 weeks ago
Modesto, California, United States CEDARS-SINAI Full timeClinical Research Associate ICedars-Sinai Medical Center is seeking a highly motivated and detail-oriented Clinical Research Associate I to join our team in the Cancer - Research Center Health Equity department.Job SummaryThe Clinical Research Associate I will work closely with a Clinical Research Coordinator, Research Program Administrator, or Research...
-
Clinical Research Associate I, PER DIEM Position
3 weeks ago
Modesto, California, United States CEDARS-SINAI Full timeJob SummaryThe Clinical Research Associate I, PER DIEM position is a part-time opportunity to work in a dynamic research environment at CEDARS-SINAI. As a key member of our research team, you will be responsible for coordinating and implementing clinical trials, ensuring compliance with protocol and research objectives.Key ResponsibilitiesCollaborate with...
-
Clinical Research Coordinator
4 weeks ago
Modesto, California, United States Vitreo-Retinal Medical Group, Inc. Full timeJob OverviewWe are seeking a highly motivated and detail-oriented Clinical Research Assistant to join our team at Vitreo-Retinal Medical Group, Inc. This is an exciting opportunity to work in a fast-paced medical office and contribute to the advancement of retina care.The successful candidate will be responsible for assisting in research patient visits,...
-
Cardiology Research Associate I
6 months ago
MODESTO, United States CEDARS-SINAI Full timeJob Description The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case report forms, entering...
-
Clinical Research Associate II
3 weeks ago
Modesto, California, United States CEDARS-SINAI Full timeJob SummaryThe Clinical Research Associate II works closely with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and implement studies. This role serves as the point of contact for external sponsors and is responsible for ensuring compliance with protocol and research objectives.Key ResponsibilitiesEvaluates...
-
Clinical Research Coordinator II
4 weeks ago
Modesto, California, United States CEDARS-SINAI Full timeJob SummaryCedars-Sinai is seeking a highly skilled Clinical Research Coordinator II to join our team in Pediatric Neonatology. As a key member of our research team, you will be responsible for providing study coordination, screening potential patients for protocol eligibility, and participating in the informed consent process.Key Responsibilities:Coordinate...
-
Modesto, CA, United States CEDARS-SINAI Full timeJob Description We are seeking a dedicated and motivated Clinical Research Coordinator with a strong background in community outreach activities, particularly within the Asian community, with a focus on the Filipino community. This role is vital in bridging the gap between our clinical research initiatives and the communities we serve, ensuring that our...
-
Clinical Research Associate I, PER DIEM
5 hours ago
Modesto, CA, United States CEDARS-SINAI Full timeJob Description Primary Duties and Responsibilities The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing...
-
Clinical Research Associate I, PER DIEM
4 weeks ago
Modesto, CA, United States CEDARS-SINAI Full timeJob DescriptionPrimary Duties and ResponsibilitiesThe Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case...
-
Clinical Research Associate I, PER DIEM
2 months ago
Modesto, CA, United States CEDARS-SINAI Full timeJob DescriptionPrimary Duties and ResponsibilitiesThe Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case...
-
Clinical Research Coordinator I
5 hours ago
Modesto, CA, United States CEDARS-SINAI Full timeJob Description Come join our team! The 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,...
-
Clinical Research Assistant
4 weeks ago
Modesto, California, United States Retinal Consultants Full timeJob Title: Clinical Research Assistant - Bilingual SpanishWe are seeking a highly motivated and detail-oriented Clinical Research Assistant to join our team at Retinal Consultants. As a Clinical Research Assistant, you will play a crucial role in supporting our clinical research department and contributing to the advancement of retina...
-
Clinical Research Assistant
1 month ago
Modesto, California, United States Retinal Consultants Full timeJoin Our Team at Retinal ConsultantsWe are a leading private medical practice specializing in the diagnosis and treatment of patients with diseases of the retina and vitreous. Our team is dedicated to providing exceptional patient care and advancing the field of retina care through innovative research and clinical trials.About the RoleWe are seeking a highly...
-
Clinical Research Assistant
4 weeks ago
Modesto, California, United States Retinal Consultants Full timeJob DescriptionWe are seeking a highly motivated and detail-oriented Clinical Research Assistant to join our team at Retinal Consultants. As a key member of our clinical research department, you will play a vital role in supporting our physicians and patients in the diagnosis and treatment of retinal diseases.ResponsibilitiesCoordinate and schedule subject...
-
Behavioral Health Specialist I
3 weeks ago
Modesto, California, United States Sierra Vista Child and Family Services Full timeJob Title: Behavioral Health Specialist IJob Summary:We are seeking a highly motivated and compassionate Behavioral Health Specialist I to join our team at Sierra Vista Child and Family Services. As a Behavioral Health Specialist I, you will work with individuals, groups, and communities to improve mental health as part of a treatment team. You will provide...
-
Modesto, United States Sutter Health Full timeJob DescriptionOrganization:MMC-Memorial Medical CenterPosition Overview: The position has the responsibility for overseeing and facilitating staff in accordance with policies, procedures, industry standards of practice, the Joint Commission (TJC) standards, and per direction of the management team. This individual assists in coordinating scrub and...
-
Modesto, United States Sutter Health Full timeJob DescriptionWe are so glad you are interested in joining Sutter Health! Organization:MMC-Memorial Medical CenterPosition Overview:The position has the responsibility for overseeing and facilitating staff in accordance with policies, procedures, industry standards of practice, the Joint Commission (TJC) standards, and per direction of the management team....
-
Modesto, California, United States TAPPI Full timeJoin Our Team of Clinical GeneticistsKaiser Permanente / The Permanente Medical Group is a leading healthcare organization with a rich history of providing high-quality medical care. Our Regional Genetics Program is a dynamic team of clinical geneticists, genetic counselors, and nurse coordinators working together to provide comprehensive genetic...
