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eTeam

Business Analyst III

eTeam, Cambridge, Massachusetts, us, 02140


Description:We are one of the most exciting pipelines in the Biotech / Pharmaceutical industry. Along with this growth comes a number of exciting opportunities to work with our expanding business areas. Within Research & Development (R&D) IT, there is a need to support the Regulatory Affairs organization team as a contract Business Analyst.This person will be expected to partner with the Principal Business Analyst and the Regulatory organization to support a suite of systems.

The key activities for this position include:

Lead/Co-Lead requirements elicitation sessionsDevelop process knowledge to translate to business and technical requirementsDocumentation of business processes and use casesAuthor of SDLC deliverables for reviewWhen required, support complex data migration activities, including Excel data mapping and repeated load processing activitiesProvide appropriate technical/functional software support throughout the life of the projectAssist in testing preparation and implementation of new applicationSupport development of training materials and facilitation of end user training sessionsContribute to the creation of operational support documentationDetermine systems retirement/data archiving requirements and execute via standard processes, as neededComplete other ad hoc tasks requested of Principal Business Analyst

Qualifications:

Strong interpersonal and teamwork skills, with the ability to interact with business users, technical IT groups, project managers, senior management, outsourced service providers, and vendors.5+ years' experience as a business analyst, with command of business analysis techniques & tools, as well as SDLC & iterative systems development methodologies.Excellent oral and written communication skills; able to organize and present ideas in a convincing and compelling manner.Ability to operate effectively in a matrix environment; team player yet able to work independently with minimal direction.Familiarity with GxP, CFR 21 Part 11 and systems validation.Life Sciences, Biotech or pharmaceutical industry experience preferred.Regulatory and/or Parexel Insight Manager knowledge a plus.

Education:BA or BS required and 5+ years of experience.