Technical Lead III

Duration: 9+ Months

The resource will oversee a system integration activities and design solutions.

Will work with a PM to ensure technical delivery. Must have knowledge of technical workstreams, architecture knowledge and design, GXP standards, SAS studio and Medidata EPC system.

Though there is an education requirement the manager has stated that experience is preferred over education.

Application Design, Architecture and Development experience in Biotech/Pharma industry.

IT Development/Technical management experience.

Experience working with outsourced service providers a plus.

Experience working with offshore delivery teams a plus.

Excellent written and communication skills; consultative skills and mentality; good listening skills with ability to make timely well-informed decisions; ability to translate business requirements and architecture designs into system designs; ability to track project activities and track progress to business value realization, escalating where necessary, hands-on experience configuring, validating, and supporting Documentum, eTMF, clinical data management systems, and drug safety systems.

Requires Bachelor's Degree in Information Technology, Computer Systems and 6+ years of experience.

Additional Job Requirements   

Responsibilities:

• The primary responsibility will be to integrate the two SAS environment into one (On-Prem Windows SAS to SAS Studio in AWS)

• Knowledge of SAS programs with moving the data/datasets

• Work with Project team to and define best way to move the closed study data to 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

Key Skills

• Should have 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

Education:

Bachelor’s degree

Shift: 1st Shift (M-F)