Development and execution of data privacy and regulation adherence frameworks, data ethics and ethical standards in data science\engineering for all aspects of the DI COE.
February 12, 2020
Demonstrated ability to understand and discuss technical concepts, manage tradeoffs, and evaluate opportunistic new ideas with internal and external stakeholders.
May 07, 2020
Provide ongoing operational support for Medidata RAVE activities during clinical trial conduct including development of clinical databases and associated external data transfer documents including import/export agreements and data specifications.
June 20, 2020
Participate in development of a protocol/study from draft status to optimize the collection of accurate and high-quality data.
July 04, 2020
Manage the overall cross-product backlog for platform requirements, drive alignment across teams and communicate status and progress.
July 20, 2020
Understand competitor landscape trends in the market as well as other ecosystem players and technology partners.
July 23, 2020
Lead a team that acts as the central resource and driving force for the design, process, manufacturing, test, quality and marketing of product(s) as they move from conception to distribution.
August 11, 2020
Collaborate with creative design, product, engineering, QA, customer success/support, field, product marketing teams across various groups to develop and evolve core platform end user engagement.
August 18, 2020
Review and contribute as a member of the CRF development team to develop the data collection modules on assigned studies where protocol requirements are outside of standard CRF library versions.
August 23, 2020
Building products that had a high level of customer centric workflow and creative design components is a plus.
September 07, 2020