Victoria Watson

Responsible for executing end to end data management activities for clinical trials, including but not limited to; data integrity review and reconciliation, query management, data management tool and system development, database lock preparation, and collaboration with investigational site staff.

• Supported multiple studies throughout my career with Merck- MK3475-991, 641, B15, 866 UNB (current), and 676 (current).
• Supported 2 DBLs with 676, and 1 DBL with B15.
• Experience with conducting UNB DVQA (MK3475-867)
• Successful mentorship of a colleague within the Nov 2022 new-hire Cohort
• Communication and collaboration with CRA, Clinical, and Medical Monitoring contacts
• Ability to adapt and learn new tasks quickly without compromising data integrity
• Team-player who is willing to volunteer for and accept additional responsibility in order to ensure study team and company success

Additional Role-specific experience:

• PK/ADA Reconciliation
• Query status and query distribution
• ROC report run and distribution
• External Vendor report running and review
• Running / Comparing reports
• Mentoring
• Super Runner POC
• MPR Review
• Manager Escalations
• Supporting Document Updates
• EVD workbook prep
• TQ006 DRC distribution
• PI signature
• Batch Number Reconciliation
• Participation in site calls to help with query resolution
• Contribution in Medical Monitoring meetings

Single point of accountability for finalizing all sales deals in the company's database, as well as all support and management responsibilities for the Accounting office.

This includes, but was not limited to;

• Managing monthly deal logs
• Balancing monthly statements
• Managing ownership and titles
• Timely (daily) monitoring of funding
• Ongoing collaboration and communication with finance and sales departments
• Contract, Invoice, payroll, and expense management