Sara Tullberg
Clinical Operations Consultant @ Hemab Therapeutics
About
In progress
-
United Kingdom
Hospital & Health Care
Data Integrity, General Data Protection Regulation (GDPR), Inspection readiness, Regulatory Inspection, Informed Consent, Paediatric trial, Timeline Development, Stakeholder Analysis, Stakeholder Mapping, Stakeholder Management, Communication, Research Ethics, Clinical Trials, Quality Assurance, MHRA, Vendor Management, Clinical Trial Management System (CTMS), Electronic Trial Master File (eTMF), Trial Master File (TMF), Change Orders
Experience
Clinical Operations Consultant
Hemab Therapeutics
Associate Director, Business Transformation
Fortrea
England, United Kingdom
Senior Project Manager
Fortrea
England, United Kingdom
Clinical Operations Consultant
30 TECHNOLOGY
England, United Kingdom
Senior Global Project Manager
Labcorp
England, United Kingdom
Contract Project Director and Operations Consultant
TCR-Solutions
England, United Kingdom
Associate Project Director
Parexel
England, United Kingdom
Senior Project Lead
Parexel
United Kingdom
Project Manager
ICON plc
England, United Kingdom
Lead CRA
ICON plc
England, United Kingdom
Clinical Research Associate (CRA)
ICON plc
England, United Kingdom
Postdoctoral Research Fellow
University of Portsmouth
England, United Kingdom
Education
University of Southampton
Pharmacology and Toxicology
University of Southampton
Pharmacology
Sara Tullberg's Contact Information
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