Senior Consultant, VAP

Description

• Lead analysis of primary and secondary data to generate meaningful value, access, pricing insights and recommendations for our clients (biopharmaceutical / pharmaceutical companies) across US payer and stakeholder types, including both qualitative (e.g., IDIs, focus groups, ad-boards) and quantitative project work.
• Train and mentor more junior staff during projects, in internal training efforts, and through formal / informal mentorship.
• Support team members by both coordinating and guiding the work of more junior staff members and effectively communicating as a partner to project managers and leadership.
• Create and present client-ready materials, including research materials, interim deliverables, and final project reports.
• Provide thought leadership in evidence strategy, value, market access and pricing in both client- and non-client-related activities (e.g., external conferences).
• Support business development activities (e.g., proposal writing) as training for future role as a BD lead.
• Support the growth of the EVAP function through involvement in internal initiatives focused on consultant’s professional development, training, and resources.

Requirements

• Strong oral and written communication skills in English language
• Ability to work under the pressure of deadlines and manage multiple priorities
• Strong team player, ability to work with cross-functional staff
• Working knowledge of essential and advanced consulting methodologies, tools, and techniques
• Excellent analytical skills and numeric capability
• High attention to detail with superior organizational and time management skills
• 3-4 years as a top performer within a top-tier biopharmaceutical / pharmaceutical strategy consulting firm serving industry leading clients on US-related business questions
• Deep knowledge of the US healthcare system and pricing dynamics, with demonstrated understanding of different payer / provider types (and related access nuances), as well as trends within the US industry
• General understanding of systematic review methods, clinical research design, and applicable standards and regulations for clinical trials
• Proficiency in MS Office Suite (Microsoft Word, PPT, and Outlook)
• Ability using PubMed / Medline, Google Scholar, research platforms to source reimbursement data

Benefits

Training + Development

Interview process

Visa Sponsorship

Security clearance