Clinical Research Associate I - Butte Lab - Department of Neurosurgery (Per Diem)

Cedars-Sinai Medical Center

Los Angeles, CA

JOB DETAILS
SKILLS
Adverse Events, Biomedical Engineering, Clinical Data, Clinical Data Collection, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Contact Management, Cross-Functional, Data Entry, Electrical Engineering, Entrepreneurship, HIPAA (Health Insurance Portability and Accountability Act), IRB/IEC (Institutional Review Board/Independent Ethics Committee), Legal, Maintain Compliance, Mechanical Engineering, Medical Equipment, Medical Imaging, Neurosurgery, Optical Engineering, Pathology, Patient Confidentiality, Patient Follow-up, Photonics, Project/Program Coordination, Regulations, Regulatory Submissions, Research Administration, Research Laboratory, Research Nursing, Sample/Specimen Processing, Startup, Team Player, Time Management, Translational Research
LOCATION
Los Angeles, CA
POSTED
30+ days ago

Job Description

When the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai. We invite you to consider this phenomenal opportunity!

Dr. Pramod Butte, Ph.D. is looking for a Clinical Research Associate I to join a diverse team! The primary focus of the Butte Laboratory is translational research in the field of bio-photonics. The Butte Lab is developing novel intra-operative imaging/visualization technologies to aid surgeons in achieving near-complete tumor excision. To learn more about the Butte Lab, please visit this website.

Serving as a Clinical Research Associate at Cedars-Sinai, you will assist in the effort in validating the clinical trial of groundbreaking medical imaging systems. The job will provide an outstanding opportunity to work with a multidisciplinary team involving optical engineers, mechanical engineers, electrical engineers, biomedical engineers as well as surgeons, pathologists, and other medical personnel. You will be involved in the development and possible commercialization of a novel medical device technology. Interest or experience in a start-up environment with an entrepreneurial spirit is highly desired.

The position will provide experience as a part of a highly focused team on a broad array of technologies. In addition, the position will also offer experience with other technicians, with clinical trials, collecting clinical data, and play a crucial part in developing clinical protocols. The position will provide opportunity to work on medical technology with far-reaching and immediate impact on patients lives.

The CRA I member will work directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. This role evaluates and abstracts research data and ensures compliance with protocol and research objectives.

Position Responsibilities

Schedules patients for research visits and research procedures.

Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.

Provides supervised patient contact or patient contact for long-term follow-up patients only.

Assists 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.

Responsible for sample preparation and shipping and maintenance of study supplies and kits.

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.

Department-Specific Duties and Responsibilities

Obtains patient consent, if authorized, to participate in clinical study.

Engages with OR staff to ensure informed, accurate, and timely transport, scanning, and processing of specimens in the context of the clinical study.

Works with, handle, and process fresh and fixated specimens per outlined protocol.

Performs scanning of specimens using clinical prototypical imaging device(s).

Performs transport, set-up, tear-down of clinical equipment used in clinical study.

Qualifications

Education:

High School Diploma or GED, required.

Experience and Skills:

Understanding of general research objectives.

Experience in a clinical research setting is highly preferred.

About the Company

C

Cedars-Sinai Medical Center

Cedars Sinai is one of the largest nonprofit academic medical centers in the United States, and it is the largest private academic medical center in the Western United States. The Cedars Sinai main campus, which encompasses nearly 24 acres, is located at the point where the cities of Los Angeles, Beverly Hills, and West Hollywood meet. Cedars Sinai has been recognized annually by U.S. News & World Report’s top 10 best hospitals in the U.S. The institution most recently placed No. 7 among a select group of 20 Honor Roll hospitals and ranked nationally in a dozen specialties. In addition, Cedars Sinai ranked No. 3 in California and No. 2 in the Los Angeles metro area.

Within Cedars Sinai, the Institute for Research on Health Aging conducts multi-disciplinary research that prioritizes the prevention of cardiovascular disease, neurocognitive disease, and cancer. Our focus is on translating new research discoveries into pragmatic interventions aimed at promoting healthy aging across diverse populations. Our approach involves human physiology, cohort, and clinical trial studies and our team includes established experts in population, clinical, translational, basic, and data science.

COMPANY SIZE
10,000 employees or more
INDUSTRY
Other/Not Classified
WEBSITE
http://www.cedars-sinai.org