As Director of Product Management at Medidata working on our data platform, I lead a team of high-performing individuals working on some of the most challenging problems in clinical trials. We are committed to harnessing cutting-edge technologies that fundamentally transform the way clinical trial data is accessed and utilized:GraphQL: To empower our users with unparalleled flexibility and customization in their access to vital clinical trial data.Semantic Technologies: Leveraging semantic technologies, we've breathed new life into structured data, transforming it into actionable insights and powering new data experiences.Our team uses Shape Up methodology, a development philosophy that enables us to deliver high-impact features efficiently. This approach ensures that we remain agile and responsive to the ever-evolving needs of our users and stakeholders.As Director of Product Management, my role encompasses various responsibilities:Strategy & Vision: I spearhead the development of a robust data platform strategy to expedite and enhance clinical trials through data-driven insights.Product Roadmap: Crafting a dynamic product roadmap that constantly integrates user feedback, market trends, and agility to solve user struggles.User-Centric Approach: We obsessively consider the unique needs of researchers, clinicians, and clinical trial professionals. Their success is our success.Thought Leadership: Staying ahead of industry trends is a perpetual responsibility. Sharing insights with our team and the broader clinical trials community is a privilege I deeply value.Making a Tangible Impact: Our work transcends technology; it's about enhancing lives through expedited, efficient, and more impactful research in clinical trials.

• Defined the vision and roadmap for future product strategy • Researched and selected technologies to be used as core product components • Promoted ways of working for product development such as design thinking, design sprints, and devops principles and methodologies • Prioritizited human factors and user-centered design both internally and to external clients • Defined data architecture and data modeling strategies for products • Developed various internal productivity tools including purpose built docker images and Slack bots • Rapidly created prototypes to show proof of concepts for the usage of various technologies and/or new ways of solving persistent problems

• Managed a team of six remote life science consultants with responsibility for up to 20 concurrent client projects • Sales activities including providing expertise to prospective clients and contract authoring • Sponsorship of projects; responsible for client stakeholder management and project delivery • Define the vision and strategy of the life sciences practice including internal culture and suite of service offerings • Responsibility to stay current with trends both inside and outside the industry for incorporation into the life sciences strategy • Finding and recruiting talent of various backgrounds to grow the life sciences practice from ~5 in 2011 to 26 consultants

My role as a Principal Life Sciences Consultant included: • Developing and freely distributing a R (Shiny) based tool for analysis of clinical data based on industry data standards • Oversight of teams of consultants and technologists on client projects • Preparation of written deliverables to clients • Engaging with other parts of the dWise business (sales, operations, billing, project management) • Development of custom solutions for clients in areas of technology, process, and management

• Global lead of a 50+ member, multi-disciplinary team in charge of co-developing and implementing a new clinical data repository and statistical computing environment within the newly merged Genentech/Roche organization• Co-lead and project managed a team to coordinate all biomarker data collection, storage, and analysis across Genentech/Roche research and development• Assisted in the interpretation and compilation of internal standards complying with the CDISC CDASH, SDTM, and ADaM metadata standards

• Statistician on Phase 1-3 studies in HIV and respiratory therapeutic areas• Statistical representative working with clinicians to develop a brand new Oncology therapeutic area beginning with a genetically targeted therapy to treat NSCLC • Programming lead on successful HIV submission to FDA and EMEA• Key user on primary analysis system and statistical user representative on partnered development of next-gen replacement