Senior Director (Expert Consultant), Real-World Evidence and HEOR Strategy

Princeton Biopartners; United States; Remote; USD 110,000 - 130,000; Part time

Job summary

An established industry player is seeking a Senior Director (Expert Consultant) to lead real-world evidence and health economics strategies. This part-time contractor role offers flexible working conditions and the opportunity to engage with biopharma innovators on strategic projects. You will leverage your extensive experience to shape evidence generation strategies and deliver high-impact solutions. Join a forward-thinking firm that values your expertise and provides a platform for professional growth while working on transformative projects in the life sciences sector.

Benefits

Flexible working model

Project-based compensation

Professional development opportunities

Qualifications

• 10+ years of experience in RWE, HEOR, or evidence generation strategy.
• Strong client-facing experience with executive presence.

Responsibilities

• Design and execute Integrated Evidence Generation Plans.
• Lead the development of RWE and HEOR strategies for clients.

Skills

Real-World Evidence (RWE)

Health Economics and Outcomes Research (HEOR)

Client-facing Experience

Analytical Skills

Strategic Thinking

Communication Skills

Entrepreneurial Mindset

Education

PhD, MD, or PharmD

Master's in a relevant STEM field

Job description

Senior Director (Expert Consultant), Real-World Evidence and HEOR Strategy

Senior Director (Expert Consultant), Real-World Evidence and HEOR Strategy

Join Princeton Biopartners as anExpert Consultant (Director-level)and help shape the future of real-world evidence and health economics strategies for leading biopharma innovators, with the flexibility to define your own projects and working model.

Princeton Biopartners is a best-in-class provider of integrated consulting solutions to the life sciences sector. Our mission is to improve the evidence base, accessibility, and awareness of biomedical innovations through strategic advisory and software solutions. We have built a reputation as a market leader in integrated evidence generation planning through our consulting solutions and tech-enabled services. Our gold-standard methodologies and best-in-class client feedback consistently recognize us as a trusted strategic partner across the biopharma industry. We are redefining how life sciences companies solvemedical affairs, evidence, and access challengesthrough integrated, transformative projects and long-term partnerships.

We are looking for a highly accomplishedSenior Director (Expert Consultant), Real-World Evidence and HEOR Strategyto join our strategic services teamon a flexible, part-time contractor basis. This is a unique opportunity for an experienced industry leader seekingproject-by-project engagementwith flexible working conditions.

As a Senior Director (Expert Consultant), you will be critical in designing and executing Integrated Evidence Generation Plans and supporting the implementation of critical HEOR and RWE tactics.You will be integral to project execution that combines our strategic insights with tech-forward solutions, ensuring clients receive end-to-end deliverables. You will join as a subject matter expert and thought leader, helping shape evidence generation strategy and tactical execution for a variety of mid-sized and large biopharma companies.

Please note: This is apart-time external contractorrole,negotiated on a project-by-project basis.

Must Haves:

• Based in the United States (remote-first), with a preference for East Coast working hours
• Advanced degree (PhD, MD, PharmD, or Master’s in a relevant STEM field preferred)
• Minimum of10 years of direct industry experiencein RWE, HEOR, or evidence generation strategy (biopharma or consulting)
• Recognizedsubject matter expertisein RWE, HEOR, or market access strategy
• Strong client-facing experience with an executive presence and polished communication skills
• Ability to act as athought leader and strategic advisor, shaping evidence generation strategies across a variety of mid-sized and large biopharma companies
• Actively seekingflexible,project-based external consultingopportunities (not a full-time employment role)
• High analytical rigor, critical thinking, and a solution-oriented mindset
• Familiarity with payer, HTA, or healthcare policy considerations (US and/or global) is a plus
• Entrepreneurial mindset with the ability to thrive in a fast-paced, flexible consulting environment

Key Responsibilities:

• Serve as asenior subject matter expert and thought partnerto biopharma client teams, shaping evidence generation strategy and execution
• Lead the development of integrated RWE and HEOR strategies that address complex client needs across a variety of therapeutic areas
• Design and execute Integrated Evidence Generation Plans, and develop and implement critical HEOR and RWE tactics (e.g., observational studies, pragmatic trials, external control arms, RWE-based HTA submissions) to drive strategic objectives
• Lead the design, prioritization, and delivery of HEOR and RWE tactical activities aligned with client priorities
• Stay abreast of the latest trends, regulatory frameworks, and best practices guiding the increasing use and acceptance of real-world evidence globally (e.g., FDA RWE Framework, EMA RWE initiatives, NICE RWE guidance)
• Engage directly with client leadership teams to diagnose challenges, co-develop solutions, and drive strategic implementation
• Synthesize scientific, clinical, and economic data into actionable, high-impact strategic recommendations
• Manage project execution from strategic scoping through final deliverable presentation, ensuring excellence at each stage
• Guide the consulting team in the development of crisp, high-level leadership presentations that drive client decision-making and organizational alignment
• Help evolve Princeton Biopartners’ consulting frameworks, methodologies, and service offerings to meet emerging client needs
• Competitive project-based compensation
• Highly flexible working model tailored to part-time availability
• Opportunity to work on strategic, high-impact projects with leading biopharma clients
• Professional development opportunities through exposure to innovative, tech-enabled consulting solutions

We do not discriminate based on race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

Seniority level

• Seniority level

  Director

Employment type

• Employment type

  Contract

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