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Business Analyst
Job in
Durham, Durham County, North Carolina, 27703, USA
Listed on 2026-02-14
Listing for:
Insight Global
Full Time
position Listed on 2026-02-14
Job specializations:
-
IT/Tech
Data Analyst, Data Science Manager
Job Description & How to Apply Below
Overview
An Insight Global client seeks to engage an experienced Business Analyst (BA) with strong expertise in Pharmaceutical Research & Development, specifically in biopharmaceutical research / clinical development / data platforms. The BA will support the client's mission to deliver innovative HIV treatments by driving high-quality business analysis across transformation initiatives and digital programs within the client's R&D and Medical organizations.
The BA will support process analysis, requirements gathering, solution and data design, user engagement, and delivery coordination across the client's R&D functions and GSK R&D Tech, including Biostatistics, Discovery, Early and Late Development and Evidence Generation. Activities include:
Responsibilities- Facilitating workshops and interviews with the client's scientific, clinical, and digital stakeholders.
- Mapping current-state and future-state R&D processes aligned to client standards.
- Eliciting and documenting requirements (business, functional, non-functional, data).
- Supporting evaluation and design of digital solutions including clinical systems and R&D data environments.
- Supporting UAT, validation, and deployment following GxP expectations.
- Contributing to change management, training, and communications.
- Business Requirements Document (BRD).
- User stories and acceptance criteria.
- Process maps aligned with client architecture standards.
- Data models and flow diagrams where needed.
- Vendor/solution assessments.
- Weekly or biweekly status reports.
- 3-5 years+ as a business analyst, solution architect, technical product / program manager, etc. in pharma R&D, clinical research, Tech Bio or other applicable environments with substantial knowledge of drug development.
- Knowledge of clinical trial systems, safety/PV platforms, regulatory information systems, and data platforms.
- Knowledge of clinical, safety, regulatory data standards.
- Strong communication and cross-functional facilitation skills.
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