• Manages a dynamic cross-functional team comprising of designers, animators, social media content strategists, UX researchers and writers to plan, develop requirements and implement numerous design projects.

● Mentored and trained team members in all aspects of clinical data management, resulting in a notable 90% increase in employee efficiency during daily operations.● Delivers supervisory support to junior team members, fostering a collaborative and efficient work environment.

• Collaborated with design and engineering teams to ensure the successful implementation and timely delivery of product features and functionalities. • Conducted user surveys and competitive analysis to inform product development decisions. • Developed user personas, user stories, scenarios, and acceptance criteria to guide the product development process. • Utilized Jira and Whimsical to create product roadmaps for sprint planning, monitored the progress of cross-functional teams through daily standup meetings, and conducted sprint reviews at the end of each sprint to evaluate accomplishments and gather feedback. • Created comprehensive product requirements document that outlined the product overview, problem statement, competitive analysis report, success metrics, user flow, and other product information. • Created wireframes using Miro, Figma and FigJam to visually illustrate and communicate product ideas.

●Oversees and coordinates numerous clinical trial projects and deliverables, while acting as the primary liaison for cross-functional team collaboration. ● Manages direct reports, ensuring the achievement of key performance indicators (KPIs) and maintaining a high standard for project execution, maintenance, and completion. ● Drafts specifications for database build and collaborates closely with developers to execute the features outlined in the specification documents. ● Performs User Acceptance Testing (UAT) of study databases, encompassing validation of data entry interfaces, edit checks, and other functionalities during database build and post-production migration. ● Conducts Vendor Reconciliation of Serious Adverse Events (SAEs), Central Laboratory Data, ECGs, and Imaging data using Microsoft Excel to ensure accuracy. ● Authors essential clinical data management documents, including electronic Case Report Forms (eCRF), Data Management Plan (DMP), eCRF Completion Guidelines (CCG), Data Validation Specification (DVS), and Data Transfer Specifications (DTS) using Microsoft Word. ● Reviews clinical trial data on an ongoing basis to ensure quality data and performs query management for the resolution of identified discrepancies. ● Monitors and visualizes study data for the identification of issues and trends using Medidata 360 reports, Tableau, PowerBI, and creates custom reports using IBM Cognos, J-Review and Business Objects

● Led cross-functional teams in end-to-end clinical data management activities, from product launch to database lock. ● Trained junior team members for increased efficiency and collaboration. ● Developed SOPs aligning data management with business priorities and compliance. ● Proactively anticipated issues and addressed data challenges with metrics-driven solutions. ● Managed user access to ensure data security and integrity across various Clinical Data Management Systems. ● Created project timelines using MS Project and SmartSheet. ● Conducted third-party vendor data reconciliation (Serious Adverse Events, Pharmacokinetics, Pharmacodynamics, Central Laboratory, and Imaging data). ● Performed User Acceptance Testing (UAT) for databases during and after Go-Live. ● Designed CDISC-aligned Case Report Forms, enhancing data collection efficacy. ● Created and updated essential data management documents and maintained study metrics reports. ● Reviewed and managed study data, queries, and reports in various EDC Systems, including Medidata Rave, Medrio, Oracle Clinical One, IBM Clinicals, DataTrak, Calyx/DataLab.