Paula Lowe

Manager, Submission Data Standards

Paula Lowe is a skilled professional, who works in Abbvie main office of which is in 95. as a Manager, Submission Data Standards from 2019. This person gained professional experience in more than eight positions at different companies. Paula Lowe went to the West Virginia University and was studying from 1992 to 1995. Paula has such professional qualifications as Certified Clinical Research Associate and Acrp. Hillsborough, North Carolina is the area, where the professional was lastly known to live. Paula Lowe's email address and phone can be accessed through SoftwareOfficial by request.
Name variants:
Paulina Lowe, Pauline Lowe, Paulie Lowe, Polly Lowe, Lena Lowe
Last updated Jun 13, 2024

Contact Information

Last Update
Jul 5, 2022
Email
pl**@gmail.com, pa**@quintiles.com
Location
Hillsborough, NC
Company

Workplace

AbbVie
Manager, Submission Data Standards

North Chicago, IL

Industry

Pharmaceuticals

Work History

Manager, Submission Data Standards

1 Waukegan Rd, North Chicago, IL 60064
from Oct 2019

Sdtm Standards Coordinator

Raleigh, NC
Create annotated case report form (aCRF) based on client SDTM dictionary Work with project team to coordinate raw data and SDTM delivery timelines Act as liaison between SDTM programmers ...
Oct 2013 — Apr 2015

Sdtm Implementation Consultant - Senior Analyst

Durham, NC
Create/Maintain SDTM annotated CRF (aCRF) Collaborate with Programming Leads to create the SDTM Programming Specifications Define the SDTM Trial Design Domains Collaborate with Programmi...
from Apr 2015

Standards Manager - Sdtm

Ucb
Act as front line point of contact for CRF design and SDTM development Review protocol and determine CRF library modules to be implemented for data collection Review and approve SDTM anno...
Jan 2013 — Oct 2013

Senior Clinical Research Associate

Ppd
929 north Front St, Wilmington, NC 28401
Conducted monitoring and site communication functions. Responsibilities included: Reviewed and tracked site reports for a team of 6 CRAs. Created monitoring plans, letter templates, train...
May 2004 — Feb 2010

Senior Project Data Manager

Responsible for all clinical data management activities for this biopharmaceutical specializing in HIV compounds. Duties included: Created and coordinated study timelines for the data, cli...
Mar 2002 — Jan 2004

Senior Clinical Data Manager

275 Grove St SUITE 101C, Newton, MA 02466
Conducted all data management tasks on 3 phase III Alzheimer’s trials which ran concurrently. Responsibilities: Created, tested and maintained validation checks Created and maintained dat...
Oct 2000 — Mar 2002

Clinical Data Specialist

North Carolina
Handled all data management work on a large NIH study and acted as line manager to a staff of 14. Responsibilities included: Tracked study progress and resource requirements, presented upd...
Jan 2000 — Sep 2000

Education

Occupations

Executive
Manager
Coordinator
Operations Manager
Managers

Skills

Oracle Clinical Edc
Phaseforward Inform Edc
Aids/Hiv
Infectious Diseases
Microsoft Office 2010
Cro
Clinical Trials
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