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.