Job summary
Job post source
This job is directly from Cedars-Sinai
Job overview
The Clinical Research Associate I at Cedars-Sinai supports clinical research studies by coordinating study activities and ensuring data accuracy and regulatory compliance within the Cancer Institute.
Responsibilities and impact
The role involves coordinating and implementing studies with clinical staff, abstracting and entering research data, assisting with regulatory submissions, patient scheduling, sample handling, and maintaining compliance with federal and institutional guidelines.
Compensation and benefits
The position offers a base pay range of $19.50 to $32.86 per hour and is classified as nonexempt with an 8-hour day shift; additional benefits are not specified.
Experience and skills
A high school diploma or GED is required, with a bachelor's degree and one year of clinical research experience preferred.
Company information
Cedars-Sinai Medical Center is a leading academic medical center with a Cancer Institute focused on research and clinical trials.
Team overview
The candidate will join the Yuan Lab within the Cancer Institute, working alongside Clinical Research Coordinators, Research Program Administrators, and Research Nurses.
Unique job features
The job emphasizes compliance with Good Clinical Practice guidelines and involves direct patient contact and regulatory responsibilities unique to clinical research.
Company overview
Cedars-Sinai is a renowned nonprofit healthcare organization based in Los Angeles, specializing in patient care, medical education, and research. It operates a highly respected hospital and numerous outpatient facilities, generating revenue through patient services, research grants, and philanthropic contributions. Established in 1902, Cedars-Sinai has a rich history of medical innovation and community service, making it a leader in healthcare advancements and a significant contributor to medical research and education.
How to land this job
Tailor your resume to highlight your experience coordinating clinical studies, data abstraction, and familiarity with regulatory compliance including IRB and FDA guidelines, as these are central to the Clinical Research Associate I role at Cedars-Sinai.
Emphasize skills in completing case report forms, entering data into electronic data capture systems, and assisting with regulatory submissions and patient research billing to align with the job responsibilities.
Apply through multiple platforms such as the Cedars-Sinai careers page, LinkedIn, and other job boards where this position is listed to maximize your application visibility.
Connect on LinkedIn with professionals in Cedars-Sinai’s Cancer Institute or research divisions; use ice breakers like commenting on recent cancer research advancements or asking about the lab’s current clinical trials to initiate conversations.
Optimize your resume for ATS by incorporating keywords from the job description such as 'clinical research coordination,' 'IRB submissions,' 'FDA compliance,' 'Good Clinical Practice,' and 'data abstraction' to ensure your resume passes initial automated screenings.
Leverage Jennie Johnson’s Power Apply feature to automate tailored applications, identify relevant job postings, and connect with Cedars-Sinai contacts, saving you time and increasing your chances of landing the role.
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