Full-time
Clinical Research Associate II - Hybrid
Competitive
Los Angeles, CAScience & PharmaceuticalPosted 19d ago
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Role overview
Job type
Salary
Competitive
Location
Sector
Posted
19 days ago
Job description
Responsibilities
Works independently under minimal direction from a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to coordinate and/or implement increasingly complex 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)
Independently prescreens potential research participants for various clinical trials. Schedules research participants for research visits and research procedures. May provide increasingly independent contact with research participants and/or conduct research participant visits independently
Assists supervising staff with regulatory submissions to the Institutional Review Board (IRB). May work directly with the Institutional Review Board to submit Adverse Events, Serious Adverse Events, Safety Letters, etc in accordance with local and federal guidelines
Assists with clinical trial budgets and patient 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
May serve as the primary point of contact for external sponsors for select trials. Responds to sponsor inquiries and attends meetings regarding study activities
Participates in and provides training and education to other Clinical Research Associates. May assist in coordinating activities of other associates to ensure compliance with protocol and clinical research objectives
Participates in centralized activities such as auditing, Standard Operating Procedure development, etc
May participate in the development of Investigator Initiated trials for Investigational New Drug applications and/or Device applications
May provide coordination of minimal number of noncomplex research studies or projects independently. May provide coverage for study coordination activities of supervising staff when needed to ensure minimal disruption to study objectives
Preferred
Bachelor's Degree in Science, Sociology, or a related field
Certification in Clinical Research, such as SOCRA or ACRP certification
Benefits
Hybrid work schedule with an expected on-site presence of 4 days per week; applicants must be able to commute to the Los Angeles work location and, if hired, must reside within a commutable distance.
Glassdoor
3.9
Since its beginning in 1902, Cedars-Sinai has evolved to meet the healthcare needs of one of the most diverse regions in the nation, continually setting new standards for quality and innovation in patient care, research, teaching and community service.
Los Angeles, California, USA
https://www.cedars-sinai.org
Late Stage
Total Funding
$64.36M
Key Investors
Google.org
California Institute for Regenerative Medicine
American Academy of Orthopaedic Surgeons
2026-01-26
Grant
2025-05-29
Grant· $1.05M
2023-12-01
Grant· $0.01M
Leadership Team
Thomas Priselac
President/CEO
David Wrigley
Executive Vice President Finance, CFO and Treasurer
Recent News
PYMNTS.com
Hospitals Follow Banks’ Playbook for Taming Generic AI
2026-07-31
EuropaWire
University of Glasgow and NHS Golden Jubilee Lead UK Role in £55 Million Women’s Heart Disease Initiative
Qualifications
High School Diploma or GED
Minimum of 1 year of clinical research-related experience
Bachelor's Degree in Science, Sociology, or a related field
Certification in Clinical Research, such as SOCRA or ACRP certification
Minimum of 1 year of clinical research-related experience.
Required skills
Represents the skills you have, click on the tags, SOCRA Certification, ACRP Certification
Preferred skills
Bachelor's Degree in Science, Sociology, or a related field
Experience
1+ years
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