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.
October 01, 2022
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 26, 2023
Manage the overall cross-product backlog for platform requirements, drive alignment across teams and communicate status and progress.
March 05, 2023
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.
March 28, 2023
Understand competitor landscape trends in the market as well as other ecosystem players and technology partners.
April 02, 2023
Demonstrated ability to understand and discuss technical concepts, manage tradeoffs, and evaluate opportunistic new ideas with internal and external stakeholders.
April 03, 2023
Participate in development of a protocol/study from draft status to optimize the collection of accurate and high-quality data.
April 18, 2023
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.
April 19, 2023
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.
April 25, 2023
Building products that had a high level of customer centric workflow and creative design components is a plus.
May 14, 2023