Krista Holsta Email
Senior Expert at Clinical Trial Department @ State Agency of Medicines of Latvia
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Krista Holsta Location
- Latvia
Krista Holsta Work
- 2019 - now Senior Expert at Clinical Trial Department @
- 2017 - 2019 Pharmacovigilance Officer @
- 2015 - 2019 Regulatory Affairs Associate Clinical Research @
- 2014 - 2019 Senior Clinical Research Associate @
- 2003 - 2014 Clinical Research Associate @
Krista Holsta Education
- Rigas Stradina Universitate
Internal medicine specialist
2006 - 2012 - University of Latvia, Medical faculty
Doctor of Medicine (M.D.) (Medicine)
2000 - 2006
Krista Holsta Skills
- Clinical Monitoring
- Protocol
- Clinical Operations
- ICH-GCP
- CTMS
- GCP
- CRO
- Clinical Trials
- Health & Safety Legislation
- Standard Operating Procedure (SOP)
- Clinical Data Management
- Pharmaceutical Industry
- Life Sciences
- Clinical Development
- Biotechnology
- Clinical Trial Management System Ctms
- Health And Safety Legislation
- Ich Gcp
- Monitoring Visit
- Clinical Research
- Good Clinical Practice Gcp
- Regulatory Affairs
- Site Initiation Visit
- Regulatory Requirements
- Pharmacovigilance
- Site Management
- Regulatory Submissions
- Standard Operating Procedure Sop
- Electronic Data Capture Edc
- Site Close Out Visit
- Good Clinical Practice
- Standard Operating Procedure
- Clinical Trial Management System
- Electronic Data Capture
Krista Holsta Summary
- Krista Holsta, based in Latvia, is currently a Senior Expert at Clinical Trial Department at State Agency of Medicines of Latvia. Krista Holsta brings experience from previous roles at Dokumeds and DOKUMEDS. Krista Holsta holds a 2006 - 2012 Internal medicine specialist @ Rigas Stradina Universitate. With a robust skill set that includes Clinical Monitoring, Protocol, Clinical Operations, ICH-GCP, CTMS and more. Krista Holsta has 1 emails on RocketReach.
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