Systems Analyst
US$105,000 – US$119,000 / yr base salary
Posted 29 Sep 2026
Advertised as “Senior Systems Analyst (R&D IT – Clinical, Regulatory, Medical)”
BranchFactor Summary
The original posting with the fluff stripped out
- Expected experience
- 5–8 yrs
- Management level
- Individual contributor
| Base salary | US$105,000 – US$119,000 / yr |
|---|
Field of studyComputer Science, Engineering, Information Systems (or related)
Study levelBachelor's
POSITION SUMMARY:
Alkermes is seeking a Sr. Systems Analyst, within the R&D IT team. This person would work closely with our Development, Clinical, Regulatory and Medical, DSPV organizations to evaluate, implement, enhance and support current systems and solutions. They will assist in optimizing data capture, data aggregation, and data analysis. The preferred candidate will utilize their experience to implement key functionality within these groups to help facilitate the development/clinical/regulatory/medical teams. Their role will include but not be limited to working with the various scientific areas to identify key data sets, facilitating the implementation of required infrastructure/solution where necessary, and working closely with the scientists and other users to understand their business needs.
All work of the Sr. Systems Analyst is conducted within regulatory guidelines and industry best practices.
Responsibilities
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Work with stakeholders to understand their business processes, requirements and data flows using various elicitation techniques
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Create and update all software lifecycle documentation
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Partner with cross functional teams including R&D, Infrastructure, Validation, QA, vendors
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Develop and manage vendor relationships, coordinating configurations, upgrades, releases, request management and support activities
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Lead data migration and curation projects as needed throughout the R&D organization
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Analyze gaps, recommend opportunities for improvement that fit the business needs
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Coordinate issue resolution with internal and external technical support providers
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Prioritize tasks between strategic initiatives, ongoing system releases and day to day activities
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Ensures adherence to regulatory requirements, cybersecurity standards, department policies, procedures and SOPs
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Build and foster effective relationships between the business stakeholders and IT
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Oversee vendor relationships for implemented systems and solutions
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Ensure adherence to FDA computer systems validation compliance
Qualifications
Minimum Education and Experience:
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Bachelor’s degree in Computer Science, Information Systems, Engineering or equivalent
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5-8 yrs experience supporting discovery, clinical, regulatory, medical organizations
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Experience in the pharmaceutical/biotech industry strongly preferred
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Hands on working knowledge of Veeva systems