Job Seekers, Welcome to SCRS Career Center
Search Filters
Use this area to filter your search results. Each filter option allows for multiple selections.
Search Results: 3381 Jobs
Create Notification
Loading... Please wait.
Tennessee Oncology Logo
Tennessee Oncology

Nashville-Davidson, Tennessee

Tennessee Oncology Logo
Tennessee Oncology

Nashville-Davidson, Tennessee

NEW! NEW!
CHRISTUS Health Logo
CHRISTUS Health

Corpus Christi, Texas

NEW! NEW!
Labcorp Logo
Labcorp

Monrovia, California

NEW! NEW!
NEW! NEW!
Labcorp Logo
Labcorp

Naples, Florida

NEW! NEW!
CHRISTUS Health Logo
CHRISTUS Health

Santa Fe, New Mexico

NEW! NEW!
Labcorp Logo
Labcorp

Portland, Oregon

NEW! NEW!
NEW! NEW!
Labcorp Logo
Labcorp

Greenville, North Carolina

NEW! NEW!
Labcorp Logo
Labcorp

Cincinnati, Ohio

NEW! NEW!
Baylor Scott & White Health Logo
Baylor Scott & White Health

Plano, Texas

NEW! NEW!
Marshfield Clinic Health System Logo
Marshfield Clinic Health System

Marshfield, Wisconsin

NEW! NEW!
NEW! NEW!
Cooper University Health Care Logo
Cooper University Health Care

Camden, New Jersey

NEW! NEW!
Marshfield Clinic Health System Logo
Marshfield Clinic Health System

Eau Claire, Wisconsin

NEW! NEW!
Northeast Georgia Health System Logo
Northeast Georgia Health System

Gainesville, Georgia

NEW! NEW!
Indiana University Health Logo
Indiana University Health

Indianapolis, Indiana

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

Fresno, California

NEW! NEW!
Sonic Healthcare USA Logo
Sonic Healthcare USA

Beaumont, Texas

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

Jacksonville, Florida

NEW! NEW!
Marshfield Clinic Health System Logo
Marshfield Clinic Health System

Iron Mountain, Michigan

NEW! NEW!
Loading... Please wait.
Clinical Research Coordinator I, Per Diem ? Thai and Asian Health Initiatives
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This job listing is no longer active.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.