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: 1568 Jobs
Save Agent
Loading... Please wait.
Kelly Science & Clinical Logo
Kelly Science & Clinical

Raleigh, North Carolina

NEW! NEW!
Kelly Science & Clinical Logo
Kelly Science & Clinical

Irvine, California

NEW! NEW!
MetroHealth

Cleveland, Ohio

NEW! NEW!
MetroHealth

Cleveland, Ohio

NEW! NEW!
MultiCare Health System Logo
MultiCare Health System

Tacoma, Washington

NEW! NEW!
Kelly Science & Clinical Logo
Kelly Science & Clinical

Titusville, New Jersey

Kelly Science & Clinical Logo
Kelly Science & Clinical

Philadelphia, Pennsylvania

University of Arizona College of Medicine-Phoenix Logo
University of Arizona College of Medicine-Phoenix

Phoenix, Arizona

Kaiser Permanente

Aurora, Colorado

Kaiser Permanente

Aurora, Colorado

Kelly Science & Clinical Logo
Kelly Science & Clinical

Santa Ana, California

Kelly Science & Clinical Logo
Kelly Science & Clinical

Irvine, California

Kelly Science & Clinical Logo
Kelly Science & Clinical

West Chester, Pennsylvania

DLH Logo
DLH

Silver Spring, Maryland

New Jersey Department of Children and Families

Trenton, New Jersey

TTF, LLC

Carlsbad, California

New York Blood Logo
New York Blood

Long Island City, New York

Luminis Health Logo
Luminis Health

Annapolis, Maryland

New Jersey Department of Children and Families

Trenton, New Jersey

Kelly Science & Clinical Logo
Kelly Science & Clinical

Irvine, California

Loading... Please wait.
Clinical Research Coordinator
Duties and Responsibilities Has knowledge of and follows good clinical practice, FDA, OHRP and HIPAA policies Serves as primary contact for research protocols as delegated by Principal Investigator (PI) Assumes responsibility of ensuring adherence and proper execution of all protocol procedures and accurate collection of data  Conducts recruitment activities as required to achieve expected study enrollment Prescreen, recruit and screen study participants and coordinate their protocol-specified study visit activities and help facilitate their continued participation Maintain subject logs and research charts in sites’ CTMS. Collect and submit source data per protocol requirements, maintaining data integrity.  Resolve queri


This job listing is no longer active.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