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: 504 Jobs
Save Agent
Loading... Please wait.
Tenet Headquarters Logo
Tenet Headquarters

Dallas, Texas

AdventHealth Logo
AdventHealth

Orlando, Florida

Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

Memorial Sloan Kettering Cancer Center Logo
Memorial Sloan Kettering Cancer Center

New York, New York

Loyola University Medical Center Logo
Loyola University Medical Center

Berwyn, Illinois

Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

Tenet Executive Search Logo
Tenet Executive Search

Town of Framingham, Massachusetts

MD Anderson Cancer Center

Houston, Texas

Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

The George Washington University Hospital Logo
The George Washington University Hospital

Washington, D.C.

Memorial Sloan Kettering Cancer Center Logo
Memorial Sloan Kettering Cancer Center

New York, New York

Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

Baylor Scott & White Health Logo
Baylor Scott & White Health

Waco, Texas

Louisiana State University Health New Orleans

New Orleans, Louisiana

Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

Rutgers, the State University of New Jersey, Logo
Rutgers, the State University of New Jersey,

New Jersey, New Jersey

University of Alabama at Birmingham

Birmingham, Alabama

Loading... Please wait.
Clinical Trials Associate II-Pediatric Genetics-FT Days
Description   JOB CODE INFORMATION: Job Code: 4646 JOB SUMMARY: Supports the activities of the Principal Investigator in accordance with the protocols and regulations. Involved in the collection, interpretation and documentation of data in support of clinical trials. Conducts off-site audits. Initiates and develops process improvements. Trains and mentors new staff members. KEY RESPONSIBILITIES: Coordinate protocol and patient consent form process. Coordinates preparation of all IRB and regulatory documents; under direction of PI may draft various communications with Sponsor. Develops assessment tool pre protocol to use in clinical researc


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