Andrew Wrong Email & Phone Number

San Carlos, California, United States

San Carlos, California, United States

South San Francisco, United States

• Secondment as Team Lead for Risk-Based Study Execution Initiative:
• Partner with Biostatistics to lead the design, development and implementation of Centralized Statistical Monitoring (automated issue detection on in-flight clinical data)
• Lead Issue Management Framework to consolidate data model and ensure end-to-end transparency

South San Francisco, United States

• Global Lead Study Manager for:- Apoptosis Program’s Colorectal Cancer and Sarcoma Cancer studies- Angiogenesis Program’s Heptocellular Cancer and Lung Cancer studies- BiTE Programs Acute Lymphoblastic Leukemia study
• Core Study Mgr Activities:- Planning, management and reporting of clinical studies- Cross-functional activities; identification & resolution of issues; and study timelines/deliverables- Planning and tracking country.
• Other activities:- Sub-Team Lead under Clinical Trial Process Optimization – Quality Analytics & Tools- Proposed, assessed, and implemented clinical analytics platform (Spotfire) for clinical data review- Member of.

South San Francisco, United States

• Working with the Study Manager to support the execution of clinical studies
• Write or contribute to preparation of clinical protocols, amendments, consent forms, study guides, CRFs, and other clinical research related documents
• Coordinate the activities associated with site start-up, including vendor management, project management, and coordination of study and implementation plans
• Assist in recruitment and approval clinical investigators
• Manage the site conduct, and overall investigational product accountability process
• Serve as the point of contact within the Therapeutic Area for study-related issues

Toronto, Canada Area

• Responsible for overall central lab management including coordination of all materials necessary for central lab sample collection
• Responsible for ensuring that design and timelines were consistent with client expectations
• Responsible for set up of trial specific documents
• Communicated and coordinated timelines for the internal and external functional units

Toronto, Canada Area

• Team Lead of database curation of a proteomics resource containing protein-protein interactions
• Met weekly deliverable publication targets
• Managed and trained staff in the assimilation of data into a publicly available online web resource
• Developed new hire training and record validation protocols
• Designed, developed and administered workflow management software
• Led the development of a data specification to store biochemical and metabolic pathway data

M.Sc., Neurophysiology

B.Sc., Neuroscience