Negotiable
Inside
Remote
United Kingdom
Summary: Insight Global is seeking a Business Consultant for a global pharmaceutical client to manage the execution and adoption of GenAI programs for R&D. The role involves collaboration with various teams to ensure successful delivery, capturing stakeholder feedback, and supporting change management efforts. This position is a long-term contract that is classified as inside IR35 and is remote based in the UK.
Key Responsibilities:
- Oversee the execution and adoption of GenAI programs for R&D.
- Collaborate with cross-functional teams including clinical operations, regulatory affairs, IT, and vendors.
- Manage scope, requirements, and success criteria for projects.
- Capture and translate stakeholder feedback into actionable improvements.
- Monitor timelines and budgets to ensure on-time, within-scope delivery.
- Proactively identify risks and propose solutions.
- Work closely with change management and training teams to support stakeholder readiness.
- Prepare regular progress updates for senior leadership.
Key Skills:
- Bachelor’s degree in Life Sciences or a related field; advanced degree preferred.
- Extensive experience in pharmaceutical R&D, clinical development, and/or regulatory affairs.
- Good understanding of systems, processes, and compliance requirements for clinical trials and regulatory submissions.
- Proven experience leading complex, cross-functional programs involving emerging technologies.
- Familiarity with Generative AI tools and implementation challenges in a regulated environment.
- Experience with Agile or hybrid delivery methodologies is a plus.
Salary (Rate): undetermined
City: undetermined
Country: United Kingdom
Working Arrangements: remote
IR35 Status: inside IR35
Seniority Level: undetermined
Industry: Other
Insight Global is hiring a Business Consultant for a global pharmaceutical client. This individual will oversee the execution and adoption of GenAI programs for R&D, starting with Paa modules and expanding across the platform. They will collaborate with cross-functional teams including clinical operations, regulatory affairs, IT, and vendors to manage scope, requirements, and success criteria. As well, they will capture and translate stakeholder feedback into actionable improvements during demos and reviews, monitor timelines and budgets to ensure on-time, within-scope delivery, while proactively identifying risks and proposing solutions. Finally, work closely with change management and training teams to support stakeholder readiness and prepare regular progress updates for senior leadership. This is a long term Inside IR35 contract and sits remotely out of the UK Must Have: Bachelor’s degree in Life Sciences or a related field; advanced degree preferred. Extensive experience in pharmaceutical R&D, clinical development and/or regulatory affairs, with good understanding of the systems, processes, and compliance requirements supporting clinical trials and regulatory submissions. Proven experience leading complex, cross-functional programs, ideally involving emerging technologies. Familiarity with Generative AI tools, platforms, and implementation challenges in a regulated environment. Experience with Agile or hybrid delivery methodologies is a plus.