Description
The Regulatory Science & Strategy (RSS) team at IQVIA supports pharmaceutical, biotechnology, and medical device companies across the product lifecycle. As an Associate Consultant, you will play a key supporting role in delivering strategic regulatory engagements, contributing to regulatory research, landscape assessments, evidence-generation planning, client deliverables, and business development support activities.
Project Delivery
- Support the execution of regulatory science and strategy consulting engagements across various products.
- Perform literature reviews, regulatory precedent analyses, and landscape assessments.
- Conduct reviews of regulatory guidance, policies, and scientific publications.
- Assist in developing evidence-generation strategies involving real-world evidence (RWE).
- Support assessments of real-world data sources and patient registries.
Analysis & Insights
- Synthesize complex scientific and regulatory information into concise insights.
- Support benchmarking activities and policy monitoring.
- Analyze publicly available regulatory documents and guidance.
Client Deliverables
- Develop high-quality PowerPoint presentations, reports, and strategic recommendations.
- Support meeting preparation, note-taking, and project coordination.
- Contribute to client-facing discussions and ensure deliverables meet quality standards.
Business & Practice Support
- Support proposal development, opportunity assessments, and thought leadership initiatives.
- Assist with preparing conference presentations, publications, and marketing content.
- Contribute to internal knowledge management and methodology development.
Qualifications
- Master's degree or equivalent in Regulatory Affairs, Regulatory Science, Epidemiology, or related disciplines.
- Bachelor's degree with demonstrated experience in regulatory affairs, consulting, or life sciences research.
Preferred Qualifications
- Experience interpreting regulatory authority guidance.
- Knowledge of clinical development, regulatory pathways, and evidence-generation principles.
- Exposure to regulatory intelligence, real-world evidence, or medical writing.
Knowledge, Skills, and Abilities
- Strong analytical and problem-solving skills.
- Ability to synthesize complex information and communicate effectively.
- Proficiency in Microsoft PowerPoint, Word, and Excel.
- Curiosity and willingness to learn in fast-paced environments.