Job Seekers, Welcome to CACRS Career Center
Search Filters
Use this area to filter your search results. Each filter option allows for multiple selections.
Search Results: 1672 Jobs
Create Notification
Loading... Please wait.
Cedars Sinai Logo
Cedars Sinai

Beverly Hills, California

NEW! NEW!
NEW! NEW!
Akron Children's Logo
Akron Children's

Akron, Ohio

NEW! NEW!
Nemours Children's Health Logo
Nemours Children's Health

Jacksonville, Florida

NEW! NEW!
UCLA Logo
UCLA

Los Angeles, California

NEW! NEW!
Veterans Affairs, Veterans Health Administration Logo
Veterans Affairs, Veterans Health Administration

Ann Arbor, Michigan

NEW! NEW!
NEW! NEW!
UCLA Logo
UCLA

Los Angeles, California

NEW! NEW!
NEW! NEW!
Cedars Sinai Logo
Cedars Sinai

Beverly Hills, California

NEW! NEW!
Cedars Sinai Logo
Cedars Sinai

Los Angeles, California

NEW! NEW!
UCLA Logo
UCLA

Los Angeles, California

NEW! NEW!
Veterans Affairs, Veterans Health Administration Logo
Veterans Affairs, Veterans Health Administration

White City, Oregon

NEW! NEW!
Veterans Affairs, Veterans Health Administration Logo
Veterans Affairs, Veterans Health Administration

Madison, Wisconsin

NEW! NEW!
Atlantic Health Logo
Atlantic Health

Newton, New Jersey

NEW! NEW!
NEW! NEW!
Fred Hutchinson Cancer Center Logo
Fred Hutchinson Cancer Center

Seattle, Washington

NEW! NEW!
NEW! NEW!
NEW! NEW!
Veterans Affairs, Veterans Health Administration Logo
Veterans Affairs, Veterans Health Administration

Huntington, West Virginia

NEW! NEW!
Veterans Affairs, Veterans Health Administration Logo
Veterans Affairs, Veterans Health Administration

Los Angeles, California

NEW! NEW!
Labcorp Logo
Labcorp

SIMZ Pudong, China

NEW! NEW!
Labcorp Logo
Labcorp

Singapore, Singapore

NEW! NEW!
Loading... Please wait.
Clinical Research Coordinator I, Goodman Lab (Hybrid)
Job DescriptionThe Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload,


This job listing is no longer active.

Check the left side of the screen for similar opportunities.
Loading. Please wait.