Real-World Evidence Scientific Lead
at Sanofi US
Dublin, County Dublin, Ireland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 15 Oct, 2024 | Not Specified | 15 Jul, 2024 | 7 year(s) or above | Pharmacoepidemiology,Heor,Pharmaceutical Industry,Biostatistics,Diabetes,Ownership,Soft Skills,Strategic Thinking,Transplant,Therapeutic Areas,Health Outcomes,Teams | No | No |
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Description:
Job title: Real World Evidence Scientific Lead - Autoimmune Diabetes
Location: Netherlands / Belgium preferred - Other European locations considered
This job offer is accessible to all, regardless of gender.
Responsibilities:
The Real-World Evidence (RWE) Scientific Lead is an essential scientific position responsible for managing the implementation of cutting-edge, effective, and efficient real world evidence strategy for the development of autoimmune type 1 diabetes (aT1D).
As such, you are responsible for the end-to-end high quality execution of real-world studies, working in close partnership with the global RWE Strategy aT1D Lead and internal and external cross functional collaborators
Your main responsibilities are as follows:
- Partner with the Real-World Evidence Strategy AT1D Lead to deliver the value of RWE for the registration, pre-launch and peri-launch of teplizumab in autoimmune type 1 diabetes.
- Manage the end-to-end planning, execution and communication of specific research studies, ensuring that deliverables are on time, within budget, to specification and of high scientific rigor that demonstrates commitment to quality.
- Deliver strategic scientific input in all stages of RWE study conceptualization through study closure, including study design, cohort construction, protocol & statistical analysis plan development, study operations, data analysis, results interpretation and clinical study report development.
- Collaborate with cross-functional stakeholders and relevant internal and external scientific experts based on specific needs of individual RWE studies to ensure that the real-world data and RWE generation is fit-for-purpose to the intended use, whether for regulatory, market access or clinical use.
- Serve as methodological expert in the design and execution of real-world study plans to address critical evidence generation gaps as well as in-house study methodology expert leveraging opportunities to use innovative RWE study designs and analytics to deliver on critical needs.
- Identify and validate external fit-for-purpose data sources, associated institutions and/or organizations, in collaboration with other members of the RWD&ES team.
- Manage the development of budgets for RWE studies in collaboration with relevant internal and external stakeholders, including RWE Operations, Sanofi Global Hub and/or vendors as appropriate, to support the annual strategic and budget planning process and periodic updates.
- Maintain timely communication and close alignment with team members, partners and stakeholders to ensure clear and timely visibility the evidence strategy, study progress and anticipation of challenges and risk mitigation.
- Accountable for supporting GenMed medical gaps within the Global Integrated Evidence Generation Plans (IEGP)
REQUIREMENT SUMMARY
Min:7.0Max:12.0 year(s)
Information Technology/IT
Software Engineering
Graduate
Proficient
1
Dublin, County Dublin, Ireland