Laryssa Lynn Stratton
age ~56
from Olive Branch, MS
- Also known as:
-
- Laryssa L Stratton
- Laryssa Buck Stratton
- Laryssa B Stratton
- Laryssa Lynn Buck
- Stratton Laryssa Stratton
- Laryssa L Buck
- Laryssa J Buck
- Lynn Buck
- David Stratton
- Phone and address:
-
14185 Hearns Cv, Mineral Wells, MS 38654
6628126964
Laryssa Stratton Phones & Addresses
- 14185 Hearns Cv, Olive Branch, MS 38654 • 6628126964
- Plano, TX
- Carrollton, TX
- Pascagoula, MS
- Wylie, TX
- Boulder Creek, CA
- Dallas, TX
- Slidell, LA
Work
-
Company:IqviaNov 2018
-
Position:Pv solutions project director
Skills
Pharmacovigilance • Pharmaceutical Industry • Drug Safety • Clinical Trials • Gcp • Regulatory Affairs • Fda • Clinical Development • Project Management • Business Planning • Strategic Leadership • Operations Management • Sop • Capa • Cro • Clinical Research • Regulatory Submissions • Gmp • Validation • Ich Gcp • Regulatory Requirements • Drug Development • Clinical Data Management • 21 Cfr Part 11 • Computer System Validation • Therapeutic Areas • Ctms • Glp • Pharmacology • Oncology
Industries
Research
Resumes
Pv Solutions Project Director
view sourceLocation:
14185 Hearns Cv, Olive Branch, MS 38654
Industry:
Research
Work:
Iqvia
Pv Solutions Project Director
Merck 2010 - 2012
Manager, Merck Consumer Care Pharmacovigilance
Merck 2010 - 2012
Director, Merck Consumer Care Pharmacovigilance
Schering Plough Healthcare 2005 - 2010
Drug Safety Surveillance Specialist
Injury Management Organization, Inc. 2002 - 2005
Utilization Review and Case Manager
Pv Solutions Project Director
Merck 2010 - 2012
Manager, Merck Consumer Care Pharmacovigilance
Merck 2010 - 2012
Director, Merck Consumer Care Pharmacovigilance
Schering Plough Healthcare 2005 - 2010
Drug Safety Surveillance Specialist
Injury Management Organization, Inc. 2002 - 2005
Utilization Review and Case Manager
Skills:
Pharmacovigilance
Pharmaceutical Industry
Drug Safety
Clinical Trials
Gcp
Regulatory Affairs
Fda
Clinical Development
Project Management
Business Planning
Strategic Leadership
Operations Management
Sop
Capa
Cro
Clinical Research
Regulatory Submissions
Gmp
Validation
Ich Gcp
Regulatory Requirements
Drug Development
Clinical Data Management
21 Cfr Part 11
Computer System Validation
Therapeutic Areas
Ctms
Glp
Pharmacology
Oncology
Pharmaceutical Industry
Drug Safety
Clinical Trials
Gcp
Regulatory Affairs
Fda
Clinical Development
Project Management
Business Planning
Strategic Leadership
Operations Management
Sop
Capa
Cro
Clinical Research
Regulatory Submissions
Gmp
Validation
Ich Gcp
Regulatory Requirements
Drug Development
Clinical Data Management
21 Cfr Part 11
Computer System Validation
Therapeutic Areas
Ctms
Glp
Pharmacology
Oncology
Youtube
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