Executive Director – Vice President, Integrated Research & Evidence Solutions

This is a fully remote position, open to applicants in United States.

📋 Description

• Act as a reliable scientific consultant for biopharmaceutical sponsors regarding Phase IV, observational, and post-approval research initiatives.

• Convert research queries into scientifically sound study frameworks, encompassing protocols, endpoints, patient demographics, data sources, and methodologies for evidence generation.

• Facilitate scientific dialogues throughout business development, which includes client interactions, discovery meetings, capability showcases, proposal crafting, and strategic solutions development.

• Establish and nurture relationships with sponsor stakeholders, serving as the main scientific point of contact during proposal creation, study design, and project commencement.

• Collaborate with Business Development, Clinical Operations, Clinical Informatics, Data Science, and Product teams to deliver integrated study solutions.

• Keep abreast of trends in epidemiology, real-world evidence, regulatory guidance, and late-phase clinical investigations.

• Represent Paradigm Health at client presentations, conferences, publications, and within industry engagements.

• Assist in generating evidence that enhances clinical practice, regulatory strategies, commercial decisions, revenue prospects, and patient outcomes.

⛳️ Requirements

• An advanced degree (PhD, DrPH, MPH, PharmD, MD, or equivalent) in Epidemiology, Public Health, Health Outcomes Research, Biostatistics, Clinical Research, or a related scientific field.

• Over 10 years of experience in designing, leading, or advising on Phase IV, observational, non-interventional, or real-world evidence studies within the pharmaceutical, biotechnology, CRO, or healthcare sectors.

• Extensive knowledge of epidemiologic techniques, study design, real-world data (RWD), and evidence generation methodologies.

• Strong comprehension of regulatory and commercial applications.

• Proven experience collaborating directly with biopharmaceutical sponsors to formulate scientific strategies and design studies that meet clinical, regulatory, market access, or commercial evidence requirements.

• Demonstrated capability to convey complex scientific ideas to varied audiences and foster trusted relationships with senior clinical, medical, and commercial stakeholders.

• Experience in supporting business development efforts, including crafting scientific strategies, making client presentations, developing proposals, and designing solutions.

• Strong understanding of the pharmaceutical development lifecycle, post-approval research, and the changing landscape of real-world evidence.

• Outstanding communication, presentation, and consultative problem-solving abilities, with the capacity to influence stakeholders and cultivate strategic partnerships.

• Established credibility through publications, presentations, professional associations, or industry leadership is preferred.

• Legal authorization to work in the United States and capability to meet U.S. visa sponsorship requirements.

🏝️ Benefits

• 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.

• Commission.