Clinical Research Coordinator II / CPT - Emergency Medicine - Full-Time, On-Site, Evenings
BEVERLY HILLS, CAPosted 17 days ago
Job summary
Job post source
This job is directly from Cedars-Sinai
Job overview
The Clinical Research Coordinator II role at Cedars-Sinai involves independent coordination of clinical research studies in emergency medicine, impacting patient enrollment and study compliance.
Responsibilities and impact
The coordinator screens patients for eligibility, manages informed consent, schedules visits, collects and reports data, ensures regulatory compliance, and supports study audits and training.
Compensation and benefits
The position offers a base pay range of $58,864 to $100,068.80, with no additional benefits explicitly mentioned in the description.
Experience and skills
Requires a high school diploma or GED, two years of clinical research experience, California phlebotomy certification, with a bachelor's degree and clinical research certification preferred; emergency department experience is desirable.
Career development
Opportunities include training and education programs, participation in quality improvement, and potential involvement in new research initiatives.
Work environment and culture
Cedars-Sinai promotes a fast-paced, high-quality care environment with a commitment to community service and innovative healthcare.
Company information
Cedars-Sinai is a leading nonprofit academic medical center known for quality healthcare, research, teaching, and community service since 1902.
Team overview
The candidate will join a large, multidisciplinary team at Cedars-Sinai, one of the largest nonprofit academic medical centers in the U.S.
Job location and travel
The job is full-time, on-site in the emergency department at Cedars-Sinai in Los Angeles, working evening shifts of 8 hours.
Unique job features
The role includes unique responsibilities like regulatory submissions, patient enrollment strategies, and participation in centralized research activities.
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
Position your resume to highlight your independent coordination skills, especially your experience screening patients for protocol eligibility and managing informed consent processes, as these are central to the Clinical Research Coordinator II role at Cedars-Sinai.
Emphasize your ability to maintain accurate source documentation, handle data collection and entry meticulously, and respond promptly to sponsor queries, showcasing your attention to detail and compliance with FDA and IRB regulations.
Apply through multiple channels including Cedars-Sinai's official career site and LinkedIn to maximize your application's visibility and reach within the organization.
Connect with Clinical Research or Emergency Medicine team members at Cedars-Sinai on LinkedIn; start conversations by referencing recent research initiatives they are involved in or asking about best practices for patient enrollment strategies in emergency medicine research.
Optimize your resume for ATS by incorporating keywords such as 'clinical research coordination,' 'protocol compliance,' 'FDA regulations,' 'IRB submissions,' 'Good Clinical Practice (GCP),' and 'patient enrollment,' ensuring your resume passes automated screenings effectively.
Utilize Jennie Johnson's Power Apply feature to automate applying across multiple platforms, tailor your resume with relevant keywords, and identify LinkedIn contacts to network with, allowing you to focus your time on preparing for interviews and advancing your candidacy.
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