RWE Director

3 days ago

London, Greater London, United Kingdom Cpl Life Sciences Full time
Evidence Strategist: Optimizing Medication Value

This is a high-level position at Cpl Life Sciences, responsible for developing and implementing evidence strategies that deliver innovative and scientifically robust evidence to Therapeutic Areas across the organization.

As an Evidence Strategist, you will serve as an expert for real world evidence (RWE) and integrated evidence, enabling cross-functional teams in becoming leaders in developing and executing integrated evidence strategies that include RWE.

The role also contributes significantly to internal enterprise-wide and external cross-stakeholder initiatives that shape our business and healthcare environments.

  • Create overarching innovative integrated evidence strategies in collaboration with internal partners to ensure the value of our medicines is fully supported by evidence.
  • Act as a thought-leader on matters pertaining to the overall creation and implementation of Innovative Medicines (IM) portfolio RWE / Integrated Evidence strategies and tactics.
  • Develop and implement new approaches to optimize approval, access, and clinical adoption of our medicines using retrospective and prospective studies.
  • Deliver high-quality, rigorous, and fit-for-purpose evidence solutions according to priorities and opportunities to impact patients and society.
  • Closely collaborate with internal and external partners ensuring scientific rigor in evidence strategy, study design, and analyses.
  • Lead partnerships with Medical Societies, Academic Institutes, payer bodies, other data owners to build meaningful RWD research collaborations.
  • Develop timely, meaningful, and robust evidence to support product value demonstration aligned with local needs (patient access, reimbursement, medical education, and patient advocacy).

Ideal Background:

  • Advanced degree or equivalent education/degree in life science/healthcare required. MBA or equivalent preferred.
  • Languages: English (oral and written)
  • 7+ years industry and/or relevant experience acquired at biopharmaceutical companies, academia, healthcare provider / Payer / HTA, or relevant consultancy companies
  • Deep understanding and experience of RWD/RWE and/or related disciplines to generate scientifically rigorous and impactful evidence.
  • Strong cross-functional experience working with Clinical Development, Commercial, Market Access, HEOR, Medical, Safety, and Regulatory colleagues.
  • Proven track record leading and executing research projects using RWD from claims, electronic health records, registries, biobanks, or digital applications, including publications.
  • Results focused, ability to meet difficult timelines in a dynamic environment

Estimated salary: up to £815 per day

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