Paula Harris Ray is a qualified expert, who works in Duke Clinical Research Institute main office of which is in 416. on the position of Clinical Data Specialist Iii from 2017. This expert gained professional experience in more than six positions at various companies. Paula Harris Ray went to the Durham Technical Community College and received education from 1991 to 1991. Durham, North Carolina is the area, where the professional was known to be settled. Paula Harris Ray's email address and number are accessed through SoftwareOfficial by request.
Name variants:
Paulina Ray,
Pauline Ray,
Paulie Ray,
Polly Ray,
Lena Ray
Last updated Jun 12, 2024
Contact Information
Last Update
Jul 7, 2022
Email
pa**@hotmail.com
Location
Durham, NC
Company
Workplace
Colleagues
Work History
Clinical Data Specialist Iii
300 west Morgan St, Durham, NC 27701
Provides input and assistance to Program Manager for scope of work changes
Provide training on procedures and systems.
Create project-related work instructions.
Maintains account...
from Sep 2017
Cda
1900 south Main St SUITE 108, Wake Forest, NC 27587
Triangle Biostatistics is a functional service provider and a biostatistics consulting organization. Our 100+ consultants have an average of 15 years of experience in the pharmaceutical indu...
Feb 2016 — Aug 2017
Principal Clinical Data Manager
Lead all activities for complex global clinical trials.
Coordinate the work of global staff assigned to the project.
Provide training on procedures and systems.
Create project-re...
Aug 2016 — 2017
Data Project Manager
450 north Sam Houston Pkwy east SUITE 250, Houston, TX 77060
Summary: Responsible for all data deliveries for assigned projects within time and budget with highest priority applied to data quality. Responsible for the planning, organization, and coord...
Apr 2013 — Jun 2015
Education
1991 — 1991
1978 — 1982
Occupations
Executive
Program Director
Artist
Model
Operations Manager
Skills
Clinical Trials
Data Management
Edc
Clinical Data Management
Cro
Gcp
Oracle Clinical
Clinical Research
Ctms
Protocol
Clinical Development
Crf Design
Pharmaceutical Industry
Ich Gcp
Oncology
Medidata
Inform
Fda
Cdisc
Good Clinical Practice
Cdisc Standards
Cro Management
Clinical Trial Management System
Electronic Data Capture