Description

Job Description:

Responsibilities:

  • The primary responsibility will be to integrate the two SAS environments into one (On[1]Prem Windows SAS to SAS Studio in AWS).
  • Knowledge of SAS programs with moving the data/datasets.
  • Work with the Project team to and define the best way to move the closed study data to the archive system.
  • Define the access, security model for SAS and Medidata environment.
  • Define, author, and present various architecture footprints i.e. Business, Logical, Integration, Security, Infrastructure, etc.
  • Adhere to Biogen SDLC methodology/process on authoring various technical deliverables.
  • Attention to detail and providing detailed documentation required in a 21 CFR validated.
  • environment.
  • Responsible for all technical delivery that includes scheduling meetings with required individuals/groups.
  • Active participation in various meetings providing technical thought process.
  • Create support transition-related documents.
  • Understanding of the Medidata EDC applications.

Skills:

  • Should have a good understanding of Clinical Study domain Pharma/Biotech.
  • Understanding of the SAS Studio and Medidata EDC applications.
  • Good understanding of Identity and Access Management protocols and technologies: OAuth, OpenID Connect, SAML, Federation, SSO such as OKTA.
  • Knowledge of various integration architectures and protocols: API Gateway, SOA, REST, XML, sFTP, MFT, WSDL, and SOAP.
  • Possess excellent problem-solving skills using creative approaches.
  • Ability to work effectively with cross-functional engineering teams and business partners.
  • Excellent written and verbal communication skills.

Requirement:

  • We are seeking a Technical Lead/Architect with knowledge of SAS software and Medidata EDC.

Education

Any Graduate