Business Analyst III
Pay Rate: $85 - $95/Hour
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 sessions
- Develop process knowledge to translate to business and technical requirements
- Documentation of business processes and use cases
- Author of SDLC deliverables for review
- When required, support complex data migration activities, including Excel data mapping and repeated load processing activities
- Provide appropriate technical/functional software support throughout the life of the project
- Assist in testing preparation and implementation of new application
- Support development of training materials and facilitation of end user training sessions
- Contribute to the creation of operational support documentation
- Determine systems retirement/data archiving requirements and execute via standard processes, as needed
- Complete 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.
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