Senior Project Biostatistics Lead- Vaccines
- Develop with other clinical/medical and global project team members the end-to-end clinical development plan for the vaccine;
- Contribute with clinical and project team members to the internal approval of the plan by governing bodies at platform (eg: RAfS) and cross platforms level (eg: STRC, CRSF, jSRC,...)
- Propose alternative trials design options, bringing innovative approaches where it adds value with the support of the Statistical Innovation team.
- Lead the cross-functional team through GO/NoGo criteria and evaluate probability of technical success.
- Propose alternative trials design options, bringing innovative approaches where it adds value with the support of the Statistical Innovation team.
- Contribute with project team members (ie: clinical, pharmacovigilance, regulatory,...) to gain Health Authorities acceptance of the plans, accountable from a statistical standpoint. Seek support from the Biostat Franchise Lead as needed.
- Oversee for his/her project the execution of the respective clinical trials: Data capture, Randomization, Statistical Analysis Plan, Analyses deliveries for primary and secondary objectives (efficacy, immunogenicity, safety). May be in charge of the most complex/priority study in the project.
- Communicate internally the trials results (Key Results Memo) and work cross-functionally (ie: clinical, safety, immunology,...) to the scientific interpretation of the results and evaluation of strategic impact on the plan.
- Contribute to the external communication of the study results to Health Authorities
- Accountable for the statistical aspects of the submission for marketing authorization or label improvement:
- ensure appropriate and quality data analyses are available efficiently to demonstrate the vaccine benefits-risks and support the label claims
- ensure appropriate and quality data analyses are available efficiently to demonstrate the vaccine benefits-risks and support the label claims
- ensure quality of the clinical data CDISC packages are delivered and comply with Health Authorities (eg: FDA, PMDA, CDE, KFDA,..) expectations
- Represent statistics in cross function working groups. Contribute to operation process optimization and provide inputs to statistics standards
- Represent Sanofi Vaccines in cross-company activities such as consortiums or professional associations
- The Senior Project Biostatistics Lead operates in a worldwide context with GBS contributors located in different sites (eg: France, US, China, India,...), with different cultures.
- The Senior Project Biostatistics Lead has no direct reports but indirect ones delivering more on the operational side, requiring the incumbent to demonstrate leadership in engaging and communicating.
- (S)He interacts with other GBS teams, Clinical, Regulatory, Global Program Head, Regulatory, Immunology, Medical Writing, Data Management
- S(H)e has regular interactions with Sr R&D Leaders in communicating complex statistical concepts. S(H)e represents Sanofi Vaccines for external activities.
- In his/her role of Senior Project Biostatistics Lead, the incumbent is accountable for all the biostatistics aspects related to the development, submission, launch and life cycle management of a medium vaccine project (5-7 clinical studies and global submission in key markets) or, a major vaccine program with support from the Biostatistics Franchise Lead.
- The incumbent will need to lead indirectly 6-12 FTEs for delivering the different project activities. S(He) makes trade-off decision on the priorities with the global project team, where there is conflict, to ensure deliveries according to Vaccines GBU scorecards. S(He) makes decision in any cross-functional initiatives where representing the platform.
- Ph.D. in Biostatistics, Mathematics or related discipline is require. Minimum 6 years biostatistics experience in pharmaceutical industry OR
- MS in Biostatistics, Mathematics or related discipline is required. Minimum 8 years biostatistics experience in pharmaceutical industry
- Proven experience in clinical development or post-marketing activities
- Demonstrate strong project management & interpersonal skills
- Broad knowledge and good understanding of advanced statistical concepts and techniques
- Able to take on the asset statistical clinical aspects through regulatory interactions, submission and marketing authorization
- Effective English oral and written communication skills
- Strive of Results
- Act for Change & Innovation
- Commit to Customers
- Cooperate Transversally
- Thinking Strategically
- Make Decisions
- Scientific Rigor, Organization skills
- Strategic Influencing skills
- Communication and Interpersonal skills
- Ability to work in a team
- Computer skills (SAS, R, Office)
- Bring the miracles of science to life alongside a supportive, future-focused team.
- Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
- Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
- Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
#LI-SP #LI-Onsite
#vhd All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
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