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Data Scientist
1 week ago
Hybrid 12-18 month contract
The Value Evidence Outcomes Scientist serves as the lead for individual projects in support of global study management: observational studies, RWE, Health Technology Assessment (HTA) processes, etc. Under the strategic lead of a Director, Value Evidence Generation & Global HTA operations and working with cross-functional teams, the Value Evidence Outcomes Scientist helps support the development of value evidence across the product life cycle in alignment with payer/HTA needs globally.
Job Responsibilities:
Develop protocols and assist in the implementation and execution (from conceptualization to development) of global VRWE studies whilst closely collaborating with global VRWE team and relevant regional stakeholders.
Provide scientific input related to HTA methodological and evidentiary requirements
Prepare and deliver proposals, technical reports, user guides, slide set presentations, conference abstracts, manuscripts, and other deliverables with guidance from the Director.
Communicate effectively with team members regarding project progress and deliverables.
Present research findings internally and at professional conferences.
Ensure compliance with all applicable internal SOPs and working practices as well as laws, regulations, and health authority guidelines.
Conduct systematic literature reviews and meta-analyses to support the development of protocols and evidence-gap analyses.
Required Qualifications:
PhD in economics/health economics, pharmaceutical outcomes and policy, statistics, biostatistics, decision sciences, health services research, biology, or a related field with a minimum of 3 years of experience in the pharmaceutical industry, contract research, or related area (including academia) OR
Master’s degree in one of the abovementioned fields and a minimum of 5 years of experience in the pharmaceutical industry, contract research, or related area (including academia).
Strong communication skills (written and oral)
Willingness to partner with cross-functional stakeholders at global and regional levels
Robust experience in project management.
Experience conducting targeted searches of the literature to identify key data or evidence
Ability to work well independently and as part of a team.
Excellent knowledge of clinical development, study designs and data interpretation
Good understanding of qualitative and quantitative approaches
Experience with both retrospective and prospective non-interventional study designs and requirements for successful study execution
Comprehensive understanding of the pharmaceutical industry and regulatory requirements from a global perspective and product development processes at all life cycle stages.
Knowledge of international healthcare systems and their changing needs for HTA submission
Highly motivated self-starter who is able to work independently, deal with complex issues and relate to multiple internal and external stakeholders.
Ideally, prior experience in RWE in oncology, nephrology, CNS and/or psychiatry
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