Clinical Research Associate I - Pulmonary Research Program/Lung Institute at Cedars-Sinai

Beverly Hills, California, United States -

Full Time

Start Date

Immediate

Expiry Date

17 Jun, 26

Salary

29.87

Posted On

19 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Data Collection, Prescreening, Scheduling, IRB Submission, Budgeting, Billing, Compliance, Data Entry, Case Report Forms, Patient Contact, Adverse Events Reporting, Sample Preparation, GCP Guidelines, HIPAA Compliance

Industry

Hospitals and Health Care

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. The Pulmonary Research team at the Cedars‑Sinai Women's Guild Lung Institute comprises a group of world-class researchers whose combined interests span multiple fields. The unified goal of this team is to understand the underlying mechanisms that cause various lung diseases and ultimately translate those findings to improve patient health. About the Role The Clinical Research Associate I will work under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies. The incumbent will support objectives of research studies through noncomplex tasks such as data collection, prescreening of and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with all federal and local guidelines. Primary Job Duties and Responsibilities: * Collects, evaluates and/or abstracts clinical research data. * May assist in designing forms for data collection/abstraction. * Enters and processes clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors. * Completes Case Report Forms (CRFs). * Schedules research participants for research visits and research procedures. Provides supervised patient contact or independent patient contact for long term follow-up patients only. * Assists supervising staff with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines. * Assists with clinical trial budgets and patient research billing. * Responsible for sample preparation and shipping and maintenance of study supplies and kits. * Ensures compliance with protocol and overall clinical research objectives. * 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. 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. 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.

Responsibilities

The Clinical Research Associate I will assist in coordinating and implementing noncomplex research studies by performing tasks such as data collection, scheduling participants, and aiding with IRB submissions. Key duties include entering data into Electronic Data Systems, completing Case Report Forms, and ensuring compliance with all federal and local guidelines.