R&D Systems Analyst — Clinical, Regulatory & Medical Tech

Experis Austria; Waltham (MA); Hybrid; USD 70,000 - 95,000; Full time

Job summary

Experis is seeking an experienced Systems Analyst to support a growing R&D technology organization within the biopharmaceutical sector in the Greater Boston area. The role requires collaboration with Clinical Development, Regulatory Affairs, Medical Affairs, Drug Safety, and other R&D functions to translate workflows into practical tech solutions.

The ideal candidate will have strong business analysis skills, hands-on Veeva knowledge, and experience in a regulated environment, with three onsite

Qualifications

• Bachelor's degree or equivalent in CS, IS, Eng, Life Sciences or related field.
• 5–8 years supporting technology solutions in R&D or life sciences.
• Experience in pharma/biotech and GxP environments.
• Hands-on experience with Veeva applications.
• Strong business and systems analysis skills with requirement facilitation.

Responsibilities

• Partner with Clinical, Regulatory, Medical, Drug Safety, and other R&D stakeholders to understand processes, requirements, workflows, and data needs.
• Translate business requirements into functional/technical specs for R&D tech solutions.
• Support evaluation, implementation, and operation of R&D applications.
• Maintain software development lifecycle and computer system validation documentation.
• Coordinate configurations, upgrades, releases, and vendor interactions.
• Lead data migration, mapping, and curation as needed.
• Ensure compliance with GxP, FDA, cybersecurity, SOPs, and validation practices.

Skills

Business analysis

Requirements gathering

Stakeholder management

Regulatory/compliance knowledge

Education

Bachelor's degree in Computer Science, Information Systems, Engineering, Life Sciences, or related discipline

Tools

Veeva

Job description

Experis is seeking an experienced Systems Analyst to support a growing R&D technology organization within the biopharmaceutical sector in the Greater Boston area. The role requires collaboration with Clinical Development, Regulatory Affairs, Medical Affairs, Drug Safety, and other R&D functions to translate workflows into practical tech solutions.

The ideal candidate will have strong business analysis skills, hands-on Veeva knowledge, and experience in a regulated environment, with three onsite