17 часов назад
Consultant, Value, Access, Pricing (Life Sciences)
96 000 - 144 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Consultant, Value, Access, Pricing (Life Sciences): Supporting life sciences consulting engagements through market research, pricing and reimbursement analysis, primary research with payers and other experts, and development of findings slides with an accent on pharmaceutical pricing dynamics, market access, and quantitative analysis. Focus on synthesizing research, recruiting and interviewing respondents, analyzing sales and pricing data, and translating complex findings into client-ready recommendations.
Location: New York, NY, United States
Salary: $96,000–$144,000 per year, plus an annual discretionary performance bonus.
Company
supports pharmaceutical, biotech, and medtech companies with life sciences commercialization consulting, therapeutic expertise, and technology-enabled solutions.
What you will do
- Prepare consulting engagements for internal and external interactions across multiple project teams.
- Conduct secondary research and develop initial hypotheses, findings, and recommendations.
- Provide therapeutic-area and market-dynamics expertise to inform project teams.
- Analyze sales value, volume, pricing, reimbursement, and other quantitative dimensions.
- Prepare, recruit for, and synthesize primary research interviews with KOLs, payers, and other relevant experts.
- Develop PowerPoint slides presenting research findings and internal team analyses.
Requirements
- 3–4 years of experience as a top performer at a top-tier biopharmaceutical or pharmaceutical strategy consulting firm.
- Deep knowledge of pricing dynamics, payer and provider types, market access, and industry trends.
- Working knowledge of consulting methodologies, tools, and techniques.
- Strong analytical, numeric, organizational, communication, and time-management skills.
- Ability to use PubMed/Medline, Google Scholar, and research platforms to source reimbursement data.
- Proficiency in Microsoft Word, PowerPoint, Outlook, and Excel, with a strong ability to collaborate across teams and manage multiple priorities.
Nice to have
- Understanding of systematic review methods, clinical research design, and standards and regulations for clinical trials.
- Interest in developing quantitative and analytical skills.
- Ability to learn quickly in a dynamic, fast-paced environment.
Culture & Benefits
- Full-time employment with formal and informal training and mentorship.
- Exposure to strategic business issues across small biotech companies and large pharmaceutical organizations.
- Opportunities to work collaboratively across multiple project teams and functions.
- Inclusion and engagement principles emphasizing connection, collaboration, shared purpose, and a respectful workplace.
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