Join our team and use your skill with an organization known nationally for excellence in research!
Joseph Schwab | About | Cedars-Sinai Medical Center
The Clinical Research Associate I works 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. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with all federal and local guidelines.
Principal Responsibilities:
Works under the direction of a Clinical Research Coordinator, Research Program Administrator or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies.
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).
Assists with prescreening of potential research participants for various clinical trials. 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.
Responsible for sample preparation and shipping and maintenance of study supplies and kits
HIPAA regulations and applicable law.
May serve as one point of contact for external sponsors for select trials. May respond to sponsor inquiries and attend meetings regarding study activity under the direction of supervising staff.
Qualifications
Education:
High School Diploma/GED is required. Bachelor's degree in Science, Sociology, or a related field preferred
Experience and Skills:
No experience required. One (1) year of clinical research related experience is preferred.
Ability to interpret and apply knowledge of State, Federal, and Agency standards to align with regulations.
Ability to convey and/or receive written/verbal information to/from various audiences in different formats.
...SUMMARY Provide soft skills training to corporate clients on an on-call basis particularly in the areas of leadership management supervisory and customer service skills and other human resource issues. Deliver training based on clients needs and objectives....
...esketamine at partner clinics. Are you ready to shape the future of healthcare? As a compassionate and dedicated Psychiatric Nurse Practitioner (PMHNP) with our team at Beckley Clinical, you will play a vital role in providing high quality psychiatric care to...
..., where precision is the standard and tungsten and molybdenum become the backbone of advanced applications. Youll walk up to a wire EDM, load the job, dial in offsets, and refine the program at the machine to turn semi-finished stock into intricate, production-ready parts...
...Role Description This is a full-time remote role for a Social Media Manager at a growing US based company. The Social Media Lead will be responsible for overseeing both the strategy and execution of social media initiatives, with a focus on driving growth, engagement...
...Babcock Power company, is dedicated to providing high-quality engineering solutions focused on electrical substations, energy storage facilities... ...you to be a part of that vision. Join Our Team As a Civil/Structural Engineer, you will play a pivotal role in the...