Current jobs related to Clinical Research Coordinator I - Modesto - CEDARS-SINAI

  • Clinical Research Coordinator I

    4 days ago

    Modesto, California, United States CEDARS-SINAI Full time

    About the RoleCedars-Sinai is seeking a highly skilled Clinical Research Coordinator I to join our team in the Department of Medicine, Endocrinology Division. As a key member of our research team, you will play a critical role in supporting the development and implementation of clinical trials, ensuring the highest level of quality and compliance with...

  • Clinical Research Coordinator I

    4 weeks ago

    Modesto, United States Cedars-Sinai Full time

    Job Description Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements!Work alongside physician-scientists and researchers who are making life-saving medical and scientific breakthroughs. Our team of scientists develop some of the most advanced clinical trials in the world.This position will provide support to the...

  • Clinical Research Associate I

    7 days ago

    Modesto, California, United States CEDARS-SINAI Full time

    Job SummaryCedars-Sinai Medical Center is seeking a highly motivated Clinical Research Associate I to join our team in the Cancer - Research Center Health Equity department. 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, and providing...

  • Clinical Research Associate I

    8 hours ago

    Modesto, California, United States CEDARS-SINAI Full time

    Job SummaryCedars-Sinai is seeking a Clinical Research Associate I to join our team in the Department of Pediatrics - Pediatric Nephrology. This part-time position will work closely with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and implement studies.Key ResponsibilitiesEvaluate and abstract clinical...

  • Clinical Research Associate I

    10 hours ago

    Modesto, California, United States CEDARS-SINAI Full time

    Job SummaryCedars-Sinai is seeking a highly motivated and detail-oriented Clinical Research Associate I to join our team in the Department of Pediatrics - Pediatric Nephrology. The successful candidate will work closely with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and implement clinical trials,...

  • Clinical Research Coordinator I

    3 months ago

    Modesto, United States CEDARS-SINAI Full time

    Job 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

    Modesto, California, United States Medix™ Full time

    Job SummaryWe are seeking a highly organized and detail-oriented Clinical Research Assistant to join our team at Medix™. As a Clinical Research Assistant, you will play a critical role in the coordination and execution of clinical trials.Key ResponsibilitiesSubject Visit Coordination: Coordinate and schedule subject visits according to protocol-specific...

  • Cardiology Research Associate I

    4 months ago

    MODESTO, United States CEDARS-SINAI Full time

    Job 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 Coordinator I

    1 month ago

    Modesto, United States CEDARS-SINAI Full time

    Job DescriptionCome 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 Coordinator I

    2 weeks ago

    modesto, United States CEDARS-SINAI Full time

    Job DescriptionCome 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 Associate I

    2 months ago

    MODESTO, United States CEDARS-SINAI Full time

    Job Description Come join our team! 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...

  • Clinical Research Associate II

    2 weeks ago

    Modesto, California, United States CEDARS-SINAI Full time

    About the RoleCedars-Sinai is seeking a highly skilled Clinical Research Associate II to join our team in the Obstetrics & Gynecology department. 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 Responsibilities:Work closely with a...

  • Clinical Research Associate I

    1 month ago

    Modesto, United States CEDARS-SINAI Full time

    Job DescriptionCome join our team!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,...

  • Clinical Research Associate I

    4 weeks ago

    Modesto, CA, United States CEDARS-SINAI Full time

    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 data,...

  • Clinical Research Associate I

    4 weeks ago

    Modesto, CA, United States CEDARS-SINAI Full time

    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 data,...

  • Clinical Research Associate I, PER DIEM

    2 weeks ago

    Modesto, CA, United States CEDARS-SINAI Full time

    Job 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

    4 weeks ago

    Modesto, CA, United States CEDARS-SINAI Full time

    Job Description Come join our team! 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...

  • Clinical Research Associate I

    4 weeks ago

    Modesto, CA, United States CEDARS-SINAI Full time

    Job Description Come join our team! 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...

  • Clinical Research Specialist II

    3 weeks ago

    Modesto, California, United States CEDARS-SINAI Full time

    Job OverviewPosition SummaryThe Clinical Research Coordinator II operates autonomously, managing the coordination of clinical studies. This includes evaluating potential participants for eligibility based on study protocols, explaining non-medical trial concepts, and facilitating the informed consent process. The role may also involve strategizing to enhance...

  • Clinical Research Specialist II

    3 weeks ago

    Modesto, California, United States CEDARS-SINAI Full time

    Job OverviewPosition SummaryThe Clinical Research Coordinator II operates autonomously to manage study coordination tasks, which include evaluating potential participants for eligibility based on study protocols, conveying non-medical trial information, and facilitating the informed consent process. This role may also involve strategizing to enhance patient...

Clinical Research Coordinator I

5 months ago

Modesto, United States CEDARS-SINAI Full time
Job 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, 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 : 1131
Working Title : Clinical Research Coordinator I - Obstetrics & Gynecology - Accortt Lab (Full-Time)
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