Tauheedah S Aquil

age ~44

from Durham, NC

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Also known as:

Tauheedah Safa Aquil
Tauheedah L Aquil
Tauheedah S Aquio
Tawheedah Aquil

Phone and address:: 104 Shadow Hawk Dr, Durham, NC 27713

Connected to:

Tauheedah Aquil Phones & Addresses

104 Shadow Hawk Dr, Durham, NC 27713
5702 Windlestraw Dr, Durham, NC 27713
5802 Tattersall Dr, Durham, NC 27713
5902 Tattersall Dr, Durham, NC 27713
Morrisville, NC

Work

Company:

Phlexglobal on assignment for pfizer
Mar 2016
Position:

Trial master file study owner

Education

Degree:

Bachelors, Bachelor of Arts
School / High School:

North Carolina Central University
1999 to 2002
Specialities:

English, Communications

Skills

Ctms • Clinical Trials • Clinical Research • Regulatory Affairs • Gcp • Sop • Cro • Ich Gcp • Edc • Therapeutic Areas • 21 Cfr Part 11 • Pharmaceutical Industry • Clinical Operations • Regulatory Documentation • Clinical Development • Ich Guidelines • Irb • Biotechnology • Sop Development • Inform • Informed Consent • Regulatory Requirements • Protocol • Gxp • Drug Development • Fda • Local Irbs • Trial Master File • Investigator Meeting Planning • Canadian Regulatory Documents • Oracle Clinical • Medical Writing • Lifesciences • Patient Recruitment

Industries

Pharmaceuticals

Resumes

Trial Master File Study Owner

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Location:

2609 Grand Ave, Waukegan, IL 60085

Industry:

Pharmaceuticals

Work:

Phlexglobal on Assignment For Pfizer
Trial Master File Study Owner
Grifols Nov 2013 - Mar 2016
Clinical Trial Assistant Iii at Grifols
Grifols Jun 2011 - Nov 2013
Clinical Trial Associate Ii
Parexel Mar 2010 - Jul 2011
Clinical Trial Specialist
Icon Plc Feb 2006 - Feb 2010
Clinical Trial Assistant

Education:

North Carolina Central University 1999 - 2002
Bachelors, Bachelor of Arts, English, Communications

Skills:

Ctms
Clinical Trials
Clinical Research
Regulatory Affairs
Gcp
Sop
Cro
Ich Gcp
Edc
Therapeutic Areas
21 Cfr Part 11
Pharmaceutical Industry
Clinical Operations
Regulatory Documentation
Clinical Development
Ich Guidelines
Irb
Biotechnology
Sop Development
Inform
Informed Consent
Regulatory Requirements
Protocol
Gxp
Drug Development
Fda
Local Irbs
Trial Master File
Investigator Meeting Planning
Canadian Regulatory Documents
Oracle Clinical
Medical Writing
Lifesciences
Patient Recruitment