Real-World Evidence Scientific Lead (Pharmacoepidemiology)
Контакты
89 200 - 118 933€
Формат работы
hybrid
Тип работы
fulltime
Грейд
lead
Английский
c1
Страна
France
aidata scienceproject managementclinical researchbiostatisticsheorreal world evidencepharmacoepidemiologyhealth outcomes research
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Чётко описанная ведущая научная роль в крупной биофармацевтической компании предполагает ответственность за исследования от начала до конца, работу с разными командами и развитие карьеры; главный нюанс - широкий охват терапевтических направлений.
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Текст:
Hirify AI/Оригинал
TL;DR
Real-World Evidence Scientific Lead (Pharmacoepidemiology): Managing end-to-end real-world evidence studies for pharmaceutical treatments with an accent on study design, healthcare data analysis, and scientific rigor. Focus on developing innovative evidence-generation methodologies, validating external data sources, and translating findings for regulatory, market access, and clinical use.
Location: Gentilly, France; hybrid work with remote work up to 2 days per week
Salary: €89,200–€118,933 per year
Company
Global AI-powered biopharma company focused on immunology, diabetes, transplant medicine, vaccines, and innovative medicines.
What you will do
Partner with Real-World Evidence Strategy Leads to deliver evidence for registration, pre-launch, and peri-launch activities across multiple therapeutic areas.
Manage the end-to-end planning, execution, communication, and closure of real-world research studies, ensuring timely delivery, budget compliance, specification, and scientific rigor.
Provide scientific input on study design, cohort construction, protocols, statistical analysis plans, study operations, data analysis, results interpretation, and clinical study reports.
Collaborate with internal and external scientific experts to ensure real-world data and evidence are fit for regulatory, market access, and clinical use.
Act as a methodological expert, identify and validate external data sources, and develop budgets with internal stakeholders and vendors.
Maintain alignment on evidence strategy, study progress, risks, and mitigation while supporting medical gaps within Global Integrated Evidence Generation Plans.
Requirements
Advanced degree in pharmaco-epidemiology, biostatistics, or Health Outcomes; a PhD is preferred. Business education is a plus.
At least 7 years of experience generating real-world evidence in the pharmaceutical industry, including end-to-end leadership experience.
Strong publication track record in relevant journals.
Experience across Type 1 diabetes, transplant, cardiovascular and metabolic disease, neurology, oncology, immunology, rare disease, insulin-based therapies, and alliance-related therapeutic areas.
Expertise in pharmacoepidemiology, HEOR, and real-world evidence study design.
Experience working with routinely collected healthcare data and managing real-world studies end to end.
Understanding of commercial strategy.
Ability to influence and motivate teams and senior leaders, with strategic thinking, ownership, urgency, and a proactive attitude.
Fluent English is mandatory.
Nice to have
PhD in pharmaco-epidemiology, biostatistics, or Health Outcomes.
Education in business.
A second European language.
Culture & Benefits
Fixed salary over 12 months with short-term incentives, profit-sharing, and bonuses based on group results.
31 days of paid leave plus RTT days, quality health insurance, and public transportation coverage up to 80%.
Maternity leave, child welcoming leave, savings and retirement plans with employer contributions, and Works Council benefits.
Remote work up to 2 days per week, internal and international mobility, and a customizable training program.
Opportunities to collaborate across science, clinical, and digital fields, work with AI and data platforms, and pursue scientific and leadership career development.
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