Associate Consultant, Regulatory Science and Strategy

IQVIA’s Regulatory Science & Strategy team supports pharmaceutical, biotechnology, and medical device clients with regulatory challenges throughout the product lifecycle. The Associate Consultant supports regulatory research, landscape assessments, evidence-generation planning, client deliverables, and business development activities.

Health Care

• Life Science
• Pharmaceutical
• Artificial Intelligence (AI)
• Accounting
• Human Resources
• Healthcare
• Publishing
• Biopharma
• Bookkeeping and Payroll
• Employment
• Freelance

Responsibilities

• Support the execution of regulatory science and strategy consulting engagements across drugs, biologics, medical devices, diagnostics, and combination products
• Perform literature reviews, regulatory precedent analyses, and landscape assessments across global regulatory agencies
• Conduct reviews of regulatory guidance, policies, public health authority communications, and scientific publications to support client objectives
• Assist in the development of evidence-generation strategies involving RWE
• Support assessments of real-world data sources, patient registries, natural history studies, and external control strategies
• Contribute to regulatory intelligence deliverables that summarize evolving regulatory expectations, precedents, and emerging trends
• Synthesize scientific, clinical, and regulatory information into concise, decision-oriented insights
• Support benchmarking activities across products, therapeutic areas, and regulatory jurisdictions
• Assist with policy monitoring and horizon scanning activities
• Analyze publicly available regulatory documents, advisory committee materials, approval packages, and guidance documents
• Develop high-quality PowerPoint presentations, reports, briefing materials, and strategic recommendations
• Support meeting preparation, note taking, action-item management, and project coordination activities
• Contribute to client-facing discussions and internal working sessions
• Ensure deliverables meet quality, scientific, and regulatory standards
• Support proposal development, opportunity assessments, and thought leadership initiatives
• Assist with preparation of conference presentations, publications, white papers, and marketing content
• Contribute to internal knowledge management activities and methodology development
• Participate in practice-wide initiatives focused on regulatory innovation, regulatory intelligence, and AI-enabled solutions

Preferred

• Experience interpreting regulatory authority guidance
• Knowledge of clinical development, regulatory pathways, and evidence-generation principles
• Exposure to regulatory intelligence, real-world evidence, epidemiology, or medical writing
• Familiarity with emerging topics such as artificial intelligence in healthcare, rare disease development, digital twins, and external controls

Benefits

• Depending on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered.
• Depending on the position offered, a range of health and welfare and/or other benefits may be offered.
• Remote work arrangement
• Lifelancer is a global platform for talent hiring in Life Sciences, Pharma, Healthtech & IT.
• London, England, GBR
• https://lifelancer.com
• Total Funding
• $0.68M
• 2025-03-01
• Pre Seed· $0.24M
• 2024-03-01
• Pre Seed· $0.11M
• 2023-03-01
• Pre Seed· $0.12M
• Leadership Team
• Jayesh Pandya
• Co-Founder & CEO
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Qualifications

• Master's degree or equivalent advanced degree in Regulatory Affairs or Regulatory Science, Epidemiology, Public Health, Health Outcomes Research, Pharmacy, Biomedical Sciences, Life Sciences, or a related discipline; OR
• Bachelor's degree with demonstrated experience in regulatory affairs, consulting, evidence generation, life sciences research, or related fields
• Strong analytical and problem-solving skills
• Ability to synthesize complex scientific and regulatory information
• Excellent written and verbal communication skills
• Strong attention to detail and commitment to quality
• Ability to work effectively within cross-functional teams
• Ability to manage multiple priorities and deadlines simultaneously
• Proficiency in Microsoft PowerPoint, Word, and Excel
• Curiosity and willingness to learn in fast-paced, evolving scientific and regulatory environments
• Comfort working in ambiguity and supporting innovative client challenges
• Experience interpreting regulatory authority guidance
• Knowledge of clinical development, regulatory pathways, and evidence-generation principles
• Exposure to regulatory intelligence, real-world evidence, epidemiology, or medical writing
• Familiarity with emerging topics such as artificial intelligence in healthcare, rare disease development, digital twins, and external controls

Required skills

• Clinical Development, Epidemiology, Evidence Generation, Medical Writing, Microsoft Excel, Microsoft PowerPoint, Microsoft Word, Real-World Evidence (RWE), Regulatory Affairs, Regulatory Guidance Interpretation, Regulatory Intelligence, Regulatory Pathways

Preferred skills

• Experience interpreting regulatory authority guidance

Experience

• Entry level