Executive Director / Vice President of Integrated Research & Evidence Solutions

Paradigm Health
United States
RemoteCareer-pivot friendly

Who this role is best for

A natural match if you have 10+ years of experience in real-world evidence and a track record of client-facing scientific partnership.

Best fit for

  • Candidates with 10+ years in real-world evidence and a history of direct sponsor collaboration
    — “10+ years of experience designing, leading, or consulting on Phase IV, observational, non-interventional, or real-world evidence studies
  • Individuals who can bridge scientific strategy with commercial outcomes and have a strong publication background
    — “Established credibility within the clinical research, epidemiology, or real-world evidence community through publications

Things to consider

  • The role demands significant client-facing time and relationship-building with senior stakeholders
    — “Serving as a primary scientific point of contact throughout proposal development
  • The position requires a deep understanding of the pharmaceutical development lifecycle and regulatory trends
    — “Strong understanding of the pharmaceutical development lifecycle, post-approval research

How to stand out

  • Highlight your experience translating research questions into study designs for sponsors
    — “Translate research questions into scientifically rigorous study designs
  • Emphasize your ability to coordinate cross-functional teams for integrated research solutions
    — “Partner closely with Business Development, Clinical Operations, Clinical Informatics, Data Science, and Product
  • Showcase your leadership in evidence generation that informs clinical and commercial decisions
    — “Generate meaningful evidence that informs clinical practice, regulatory strategy, and commercial decision-making
Pace · Fast PacedCollaboration · HighAutonomy · HighDecision Impact · TeamLevel · Executive

Derived from job-description analysis by Serendipath's career intelligence engine.

What success looks like

  • successful delivery of integrated solutions for Phase IV, observational, and post-approval research programs
  • building strong relationships with sponsor stakeholders
Typical background
epidemiologistRWE scientistlate-phase clinical research expert

Skills & requirements

Required

Scientific ExpertiseClient-facingBusiness DevelopmentProject ManagementCross-functional Collaboration

Preferred

EpidemiologyRWE ScienceLate-phase Clinical Research

About the role

Original posting from Paradigm Health via Ashby

Paradigm Health is rebuilding the clinical research ecosystem by enabling equitable access to trials for all patients. Our platform enhances trial efficiency and reduces the barriers to participation for healthcare providers. Incubated by ARCH Venture Partners and backed by leading healthcare and life sciences investors, Paradigm’s seamless infrastructure implemented at healthcare provider organizations, will bring potentially life-saving therapies to patients faster.

Our team hails from a broad range of disciplines and is committed to the company’s mission to create equitable access to clinical trials for any patient, anywhere. Join us, and bring your expertise, passion, creativity, and drive as we work together to realize this mission.

ABOUT THE ROLE:

We are seeking an accomplished Executive Director/Vice President Integrated Research & Evidence Solutions to serve as a strategic scientific partner to biopharmaceutical sponsors throughout the design, development, and execution of Phase IV, hybrid retrospective/prospective, and observational research programs. This highly visible, client-facing role is ideal for an experienced epidemiologist, RWE scientist, or late-phase clinical research expert who combines deep scientific expertise with a passion for partnering with sponsors to generate meaningful evidence that informs clinical practice, regulatory strategy, and commercial decision-making.

In this role, you will collaborate directly with sponsors to understand their evidence-generation objectives, develop scientifically robust study designs, and translate complex research needs into tailored solutions. As a trusted advisor throughout the business development lifecycle, you will support commercial discussions, contribute to proposal development and study strategy, present scientific capabilities, and partner closely with clinical operations and cross-functional teams to spearhead and coordinate successful study design solutions. Your ability to build trusted client relationships while providing strategic scientific guidance will be instrumental in advancing innovative research and driving long-term partnerships, revenue opportunities and improve patient outcomes.

WHAT YOU'LL DO:

  • Serve as a trusted scientific advisor to biopharmaceutical sponsors, partnering with clinical, medical, product, commercial, and evidence-generation teams to design and drive the creation of integrated solutions for Phase IV, observational, and post-approval research programs that address sponsor’s clinical objectives.
  • Collaborate with sponsors to translate research questions into scientifically rigorous study designs, including protocol development, endpoint selection, patient population strategy, data source recommendations, and evidence-generation methodologies.
  • Lead scientific discussions throughout the business development lifecycle by participating in client meetings, discovery sessions, capability presentations, proposal development, and strategic solutioning–inclusive of the application of Paradigm Health’s product suite–to differentiate our organization as a trusted partner in driving evidence outcomes.
  • Build and maintain strong relationships with sponsor stakeholders, serving as a primary scientific point of contact throughout proposal development, study design, and project initiation.
  • Partner closely with Business Development, Clinical Operations, Clinical Informatics, Data Science, and Product to develop innovative, integrated study solutions that meet sponsor objectives and ensure successful study execution.
  • Monitor emerging trends in epidemiology, real-world evidence, regulatory guidance, and late-phase clinical research to provide strategic insights that strengthen client partnerships and expand business opportunities.
  • Represent the organization as a scientific thought leader through client presentations, conference participation, publications, and industry engagement.

WHO YOU ARE:

  • Advanced degree (PhD, DrPH, MPH, PharmD, MD, or equivalent) in Epidemiology, Public Health, Health Outcomes Research, Biostatistics, Clinical Research, or a related scientific discipline.
  • 10+ years of experience designing, leading, or consulting on Phase IV, observational, non-interventional, or real-world evidence studies within the pharmaceutical, biotechnology, CRO, or healthcare industry.
  • Deep expertise in epidemiologic methods, study design, real-world data (RWD), and evidence generation, with a strong understanding of regulatory and commercial applications.
  • Demonstrated experience partnering directly with biopharmaceutical sponsors to develop scientific strategies and design studies that address clinical, regulatory, market access, or commercial evidence needs.
  • Proven ability to communicate complex scientific concepts to diverse audiences and build trusted relationships with senior clinical, medical, and commercial stakeholders.
  • Experience supporting business development activities, including scientific strategy, client presentations, proposal development, and solution design.
  • Strong understanding of the pharmaceutical development lifecycle, post-approval research, and the evolving real-world evidence landscape.
  • Exceptional communication, presentation, and consultative problem-solving skills, with the ability to influence stakeholders and drive strategic partnerships.
  • Established credibility within the clinical research, epidemiology, or real-world evidence community through publications, presentations, professional affiliations, or industry leadership is preferred.

WHAT YOU'LL RECEIVE:

Paradigm Health offers a comprehensive Total Rewards package to support your well-being and success, including:

  • Competitive health, dental, and vision insurance
  • Mental health support for you and your family
  • Equity package
  • Unlimited paid time off (PTO)
  • 16 weeks of paid parental leave
  • Flexible work options – remote and hybrid arrangements
  • Company-paid life insurance, short-term and long-term disability coverage
  • 401(k) plan with company match

At Paradigm Health, we are committed to providing equal employment opportunities to all qualified individuals. We encourage and welcome candidates from all backgrounds and perspectives to apply for our open positions. We are interested in all qualified individuals and ensure that all employment decisions are based on job-related factors such as skills, experience, and qualifications.

Source: Paradigm Health careers (Ashby)

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