The Association of Clinical Research Professionals

CAREER CENTER

Job Seekers, Welcome to ACRP Career Center
Search Filters
Use this area to filter your search results. Each filter option allows for multiple selections.
Search Results: 2305 Jobs
Save Agent
Loading... Please wait.
Ochsner Health Logo
Ochsner Health

New Orleans, Louisiana

NEW! NEW!
Mile Square Health Center

Chicago, Illinois

NEW! NEW!
Tallahassee Memorial HealthCare

Tallahassee, Florida

The Cleveland VA Medical Research & Education Foundation Logo
The Cleveland VA Medical Research & Education Foundation

Cleveland, Ohio

Cleveland VA Medical Research & Education Foundation Logo
Cleveland VA Medical Research & Education Foundation

Cleveland, Ohio

Ohio University Heritage College of Osteopathic Medicine opathic Me

Athens , Ohio

University of Utah

Salt Lake City, Utah

Zepto Life Technology, Inc. Logo
Zepto Life Technology, Inc.

Saint Paul, Minnesota

Cleveland Clinic Logo
Cleveland Clinic

Cleveland, Ohio

Arthrex

Naples, Florida

Sarah Cannon Research Institute Logo
Sarah Cannon Research Institute

Nashville, Tennessee

New Jersey Department of Children and Families

Trenton, New Jersey

Sarah Cannon Oncology CRO Logo
Sarah Cannon Oncology CRO

Lexington,

Sarah Cannon Research Institute Logo
Sarah Cannon Research Institute

Denver, Colorado

Sarah Cannon Oncology CRO Logo
Sarah Cannon Oncology CRO

Nationwide

Moffitt Cancer Center Logo
Moffitt Cancer Center

Tampa, Florida

Arthrex

Naples, Florida

University of Illinois Cancer Center

Chicago, Illinois

Fred Hutchinson Cancer Center Logo
Fred Hutchinson Cancer Center

Seattle, Washington

Mile Square Health Center

Chicago, Illinois

Loading... Please wait.
Clin/Tran Research Coord III
Description JOB SUMMARY: Responsible for coordinating the approval processes and conduct of research protocols, such that the integrity and quality of the clinical/translational research is maintained and the research is conducted in accordance within all policies, independently. Responsible for the timely preparation, planning and quality control of regulatory documents required for human subjects research. Supervise set-up and maintenance of biorepositories and assist in manuscript preparation. KEY RESPONSIBILITIES: Submits Informed Consent, Human Subjects' Research Applications, DSMB, HIPAA compliance, Radiation and Biosafety and other pertinent regulatory forms to the IRB for institution approval of clinical trials


This job listing is no longer active.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