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CLINICAL TRIALS OFFICE, PROGRAM COORDINATOR

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Date: Jan 30, 2019

Location: Greenville, SC, US, 29605

Company: Greenville Health System

Bilingual (Spanish / English) candidates are encouraged to apply.

Requisition # 41767 

Employment Type Full-time 

Job Class

NON CLINICAL PROFESSIONAL

FLSA

Exempt

Job Summary

Supports the Office of Clinical Research (Clinical Trials/CTMO) in the planning, implementation and analysis of efforts to improve the quality and efficiency of processes critical to conducting clinical research, implements technology solutions/systems for the administrative review and approval of research projects to ensure compliance with federal regulations and institution policies. Facilitates continuous improvement of research administration workflows by reporting on key metrics and other evaluation data. Develops training materials and tools to promote compliance and best practices.

Supervisory/Management Responsibilities

This is a non-management job that will report to a supervisor, manager, director or executive.

Minimum Education

Bachelor's Degree in a related field

Minimum Experience

3 years - research coordination / administration or project management

Required Certifications/Registrations/Licenses

NOT APPLICABLE

Specific Acceptable Credentials (if applicable)

N/A

In lieu of the Above Minimum Requirements

N/A

Other Required Experience

Lead or Coordinator experience - Required

Project Management experience - Preferred

Position Posting Category

Non Clinical Professional / Technical


Nearest Major Market: Greenville
Nearest Secondary Market: South Carolina

Job Segment: Clinic, Clinical Research, Medical Research, Project Manager, Healthcare, Technology

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