Job Description Job Summary: We are seeking an experienced and highly motivated
Business Analyst with a strong background in
Veeva RIM and regulatory publishing processes. The ideal candidate will bring solid business analysis expertise, including requirements elicitation, documentation, and test scenario development, to support the successful implementation and optimization of regulatory information management solutions.
This is a
hands-on, independent role where the Business Analyst will serve as the sole BA on the project, requiring a proactive and self-starting professional who can effectively engage with stakeholders and drive deliverables from start to finish.
Contract that goes through 12/19/25 chance to extend.
If offered the role, you are a W2 employee of Atrium.
Remote eligible
Key Responsibilities: - Engage with business stakeholders and subject matter experts (SMEs) to elicit, analyze, and document detailed business and functional requirements
- Develop and maintain comprehensive documentation including process flows, use cases, and user stories
- Collaborate with DTE (Data, Technology and Engineering) teams and business SMEs to define and validate test scenarios and test scripts
- Conduct test script reviews and facilitate dry runs to ensure solution readiness
- Act as a liaison between business and technical teams to ensure alignment on requirements and solutions
- Provide expertise and insights into regulatory publishing business processes and systems
- Work independently to manage priorities, deadlines, and project expectations
Required Qualifications: - Proven experience as a Business Analyst in the Life Sciences/Pharmaceutical industry
- Strong understanding of Veeva RIM systems and regulatory publishing processes
- Experience defining and reviewing test scripts, and coordinating testing activities
- Ability to gather and document business requirements with clarity and precision
- Self-motivated, detail-oriented, and capable of working autonomously in a fast-paced environment
- Excellent communication and stakeholder management skills
Preferred Qualifications: - Experience with Veeva Vault Submissions Publishing
- Familiarity with global regulatory compliance requirements and documentation standards
Pay Range $80-$90/HR
Requisition Disclaimer This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals ("Vertex"). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements
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If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.
No C2C or Third-Party Vendors