Sarah Wilson is Quality Assurance Expert focused on clinical research. Ms. Wilson has more than 28 years
domestic and international pharmaceutical industry experience. An experienced and successful quality assurance
professional, she offers expertise in Good Clinical Practices (GCP), Good Laboratory Practices (GLP) and Good
Manufacturing Practices (GMP). Skilled in central laboratory, CRO, IRB and vendor qualification assessments. Strong
auditing skills that identifies clear and significant improvement needs with FDA regulations and other applicable
regulatory, protocol and internal procedures. Excellent training skills used to successfully develop and implement
training programs for professional growth among peers, colleagues and other applicable industry professionals.
International experience includes Austria, Brazil, Czech Republic, Canada, Russia, Bulgaria, Poland, France, Spain
and the UK.
Specialties:
GCP Investigator Site Auditing
GCP Training
GCP Supplier Qualification and Routine Audits
Site Master File Review for GCP Compliance
Monitoring Report Review/Assessments
SOP Writing & Review
GMP Auditing & Training
Qualifying Investigators
Qualifying vendors, suppliers, central laboratories, CROs, SMOs, etc.
Hosting Regulatory Agency Inspections (US & Canada)
A Certified Clinical Research Professional and a Certified cGMP Trainer, Sarah has written abstracts and presented
posters and seminars to professionals worldwide for organizations such as DIA, SQA and SoCRA. Sarah also started
the Georgia SoCRA Chapter to bring local professionals together for training and networking.
domestic and international pharmaceutical industry experience. An experienced and successful quality assurance
professional, she offers expertise in Good Clinical Practices (GCP), Good Laboratory Practices (GLP) and Good
Manufacturing Practices (GMP). Skilled in central laboratory, CRO, IRB and vendor qualification assessments. Strong
auditing skills that identifies clear and significant improvement needs with FDA regulations and other applicable
regulatory, protocol and internal procedures. Excellent training skills used to successfully develop and implement
training programs for professional growth among peers, colleagues and other applicable industry professionals.
International experience includes Austria, Brazil, Czech Republic, Canada, Russia, Bulgaria, Poland, France, Spain
and the UK.
Specialties:
GCP Investigator Site Auditing
GCP Training
GCP Supplier Qualification and Routine Audits
Site Master File Review for GCP Compliance
Monitoring Report Review/Assessments
SOP Writing & Review
GMP Auditing & Training
Qualifying Investigators
Qualifying vendors, suppliers, central laboratories, CROs, SMOs, etc.
Hosting Regulatory Agency Inspections (US & Canada)
A Certified Clinical Research Professional and a Certified cGMP Trainer, Sarah has written abstracts and presented
posters and seminars to professionals worldwide for organizations such as DIA, SQA and SoCRA. Sarah also started
the Georgia SoCRA Chapter to bring local professionals together for training and networking.
Learn About Sarah Wilson
| (c) copyrighted 2008 |
| Quality You Can Count On, Today,Tomorrow, To Market. |
 |
 |
 |
 |