Clinical Research Coordinator I (Onsite) - Cancer Clinical Trials Office

Clinical Research Coordinator I (Onsite) - Cancer Clinical Trials Office Employer Cedars-Sinai Location Los Angeles, California Salary Competitive Closing date 25 Apr 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 job.
Job Description Onsite presence required a minimum of three days a week At Cedars-Sinai, we're motivated by a collective spirit of innovation and the challenge to continuously improve.
Above all, we share a real dedication for helping others.
Day after day, from department to department, our people give their all to create a community unlike any other.
This is just one of the many reasons U.
S.
News & World Report has named us one of America’s Best Hospitals-and now we invite you to join us and make a difference every single day in service of this outstanding work - excellence and innovation in patient care, research, and community service.
From working with a team of committed professionals to using state-of-the-art facilities, you’ll have great resources to do something incredible-for yourself, and for others! Cedars-Sinai Cancer is committed to pursuing pioneering research into disease mechanism, diagnostic innovations and new technologies and resources.
Through our historic achievements, growing research enterprise, and serving one of the most diverse regions in the world, our physicians and scientists are uniquely positioned to guide the next generation of progress against the disease.
Are you looking to contribute to groundbreaking research? We look forward to having you come and 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).
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.
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.
Performs phlebotomy services according to CSMC policies and procedures.
Verifies specimen identification, assesses appropriateness of test orders and quality of specimen by recognizing #Jobs-Indeed Qualifications Requirements: High School Diploma/GED required One (1) year of Clinical Research Related experience required Please note this is NOT a remote role, an onsite presence is required Preferred: Bachelor's Degree Science, Sociology or related degree preferred Certification in clinical Research: SOCRA or ACRP certification preferred Why work here? Beyond an outstanding benefits package and competitive salaries, we take pride in hiring the best, most committed employees.
Our staff reflects the culturally and ethnically diverse community we serve.
They are proof of our dedication to creating a multifaceted, inclusive environment that fuels innovation and the gold standard of care we strive for.
#jobs-indeed 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 : HRC0962518 Working Title : Clinical Research Coordinator I (Onsite) - Cancer Clinical Trials Office Department : Cancer - SOCCI Clinical Research 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.
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