Clinical Research Coordinator I
2 weeks 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 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 : 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
-
Clinical Research Coordinator I, SLASH
3 weeks ago
Sacramento, United States Cedars-Sinai Full timeJob Description 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...
-
Clinical Research Coordinator
2 weeks ago
Sacramento, United States Medix Full timeWe are looking for a self-starter to join our team as a Clinical Research Coordinator. We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. We are also open to those looking to relocate to California. If you're a Clinical Research professional ready to take the next step in...
-
Non-Clinical - Clinical Research Coordinator
2 weeks ago
Sacramento, United States The Fortus Group, Inc. Full timeFortus Healthcare Resources is seeking a Travel Clinical Research Coordinator Non-Clinical for an immediate opening in Sacramento, CA . Clinical, Research, Coordinator, Clinic, Healthcare, Staffing
-
Clinical Research Coordinator
3 weeks ago
Sacramento, United States Medix™ Full timeClinical Research Coordinator - Sacramento, CAA Sacramento-based Research Center is speaking an experienced Clinical Research Coordinator to join their team. This individual will be supporting mainly industry and investigator initiated psychiatric studiesResponsibilities:Recruit, enroll, and obtain informed consent from patients for clinical trials.Handle...
-
Clinical Research Coordinator
2 weeks ago
Sacramento, United States Medix™ Full timeClinical Research Coordinator - Sacramento, CAA Sacramento-based Research Center is speaking an experienced Clinical Research Coordinator to join their team. This individual will be supporting mainly industry and investigator initiated psychiatric studiesResponsibilities:Recruit, enroll, and obtain informed consent from patients for clinical trials.Handle...
-
Clinical Research Coordinator I
2 weeks ago
Sacramento, United States CEDARS-SINAI Full timeJob 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,...
-
Cardiology Research Associate I
1 week ago
SACRAMENTO, United States CEDARS-SINAI Full timeJob DescriptionThe 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...
-
Cardiology Research Associate I
2 weeks ago
SACRAMENTO, 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 Coordinator
2 weeks ago
Sacramento, United States Medix™ Full timeWe are looking for a self-starter to join our team as a Clinical Research Coordinator. We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. We are also open to those looking to relocate to California. If you're a Clinical Research professional ready to take the next step in...
-
Clinical Research Coordinator
15 hours ago
Sacramento, United States Medix™ Full timeWe are looking for a self-starter to join our team as a Clinical Research Coordinator. We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. We are also open to those looking to relocate to California. If you're a Clinical Research professional ready to take the next step in...
-
Clinical Research Coordinator
2 weeks ago
Sacramento, United States Medix™ Full timeWe are looking for a self-starter to join our team as a Clinical Research Coordinator. We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. We are also open to those looking to relocate to California. If you're a Clinical Research professional ready to take the next step in...
-
Clinical Research Coordinator II
1 week ago
SACRAMENTO, United States CEDARS-SINAI Full timeJob DescriptionThe 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,...
-
Clinical Research Coordinator I
2 weeks ago
West Sacramento, 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,...
-
Sacramento, 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...
-
Level II
1 week ago
Sacramento, CA, United States Sutter Health Full timeSutter Health is seeking a Clinical Research Coordinator Level II for a job in Sacramento, California. Job Description & Requirements Specialty: Clinical Research Coordinator Discipline: Allied Health Professional Start Date: ASAP Duration: Ongoing Employment Type: Staff We are so glad you are interested in joining Sutter Health! Organization: ...
-
Research Associate I
2 weeks ago
Sacramento, United States Cedars-Sinai Full timeJob Description Are you ready to be a part of breakthrough research? Working under direct supervision, the Research Associate I performs a variety of routine experimental protocols and procedures to support the objectives of one or more laboratory research projects in a specific area of research. Assists in general laboratory activities, including...
-
Clinical Research Coordinator 224410
15 hours ago
Sacramento, United States Medix™ Full timeResponsibilities: Coordinate daily activities for clinical trials and ensure smooth operation. Administer sponsor-required surveys. Collaborate with colleagues to manage study supplies. Train staff on study procedures and keep records of training. Create and maintain trial documents. Attend meetings as requested. Understand and review study protocols. Assist...
-
Clinical Research Coordinator 224410
1 day ago
Sacramento, United States Medix™ Full timeResponsibilities: Coordinate daily activities for clinical trials and ensure smooth operation. Administer sponsor-required surveys. Collaborate with colleagues to manage study supplies. Train staff on study procedures and keep records of training. Create and maintain trial documents. Attend meetings as requested. Understand and review study protocols. Assist...
-
Level II
1 week ago
Sacramento, CA, United States Sutter Health Full timeSutter Health is seeking a Clinical Research Coordinator Level II for a job in Sacramento, California. Job Description & Requirements Specialty: Clinical Research Coordinator Discipline: Allied Health Professional Start Date: ASAP Duration: Ongoing Employment Type: Staff We are so glad you are interested in joining Sutter Health! ...
-
Clinical Research Associate II
2 weeks ago
Sacramento, United States Allen Spolden Full timeJob DescriptionResponsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team.Essential Duties And ResponsibilitiesParticipate and assist in design and preparation of protocols and case report forms.Generate clinical SOPs, policies,...
