In This Section

Career Center

Job Seekers, Welcome to ASPET Career Center
Search Filters
Use this area to filter your search results. Each filter option allows for multiple selections.
Search Results: 567 Jobs
Save Agent
Loading... Please wait.
Wayne State University - Institute of Environmental Health Sciences/CURES

Detroit, Michigan

Missouri State University

Springfield, Missouri

Clemson University

Clemson, South Carolina

University of Arizona, R. Ken Coit College of Pharmacy

Tucson, Arizona

University of Georgia, College of Pharmacy

Athens, Georgia

Texas Tech University Paul Foster School of Medicine

El Paso, Texas

Office of Strategic Coordination, National Institutes of Health (NIH) Logo
Office of Strategic Coordination, National Institutes of Health (NIH)

bethesda, Maryland

National Cancer Institute, NIH

Rockville, Maryland

Geisinger Logo
Geisinger

Scranton, Pennsylvania

NEW! NEW!
Corporate Logo
Corporate

Los Angeles, California

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

TEMPLE, Texas

NEW! NEW!
Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

NEW! NEW!
The George Washington University Hospital Logo
The George Washington University Hospital

Washington, D.C.

NEW! NEW!
Saint Francis Hospital - Memphis Logo
Saint Francis Hospital - Memphis

Memphis, Tennessee

NEW! NEW!
Corporate Logo
Corporate

Dallas, Texas

NEW! NEW!
Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

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

Plano, Texas

NEW! NEW!
Loading... Please wait.
Clinical Research Coordinator
Job Summary: The Clinical Research Coordinator (CRC) for the WMC Cancer Center's Cancer Clinical Trials Office (CCTO) will manage clinical research studies by coordinating and participating in the collection, compilation, documentation and analysis of clinical research data. The CRC also directly interacts with study participants to monitor progress, including documenting and reporting adverse events. The CRC will be responsible for maintaining source documents and submitting case report forms as required for clinical trials and assist clinical staff with sample collection, processing, handling, and shipping as outlined in the protocol. The CRC specialist will report directly to the Medical Director of the CCTO. Responsibilities:


This job listing is no longer active.

Check the left side of the screen for similar opportunities.
Loading. Please wait.
Powered By Naylor Association Solutions