• Level:L3
• Reporting to: Medical Operations Lead Eurasia
• Location: Istanbul or MCO Countries
• Job type: Permanent

About the job

Our Team:

The Eurasia Medical Team at Sanofi is a high-performing team of Medical leaders who are a trusted source of scientific and Medical information and shared insights; effective and innovative strategic partners to our internal and external stakeholders; and dedicated to public health. We represent diverse experiences and backgrounds which strengthens our team and mirrors the healthcare communities we engage.

The Real-World Data & Evidence Science (RWD&ES) team, part of GBU Medical, serves as an end-to-end strategy and execution partner in applying RWE and data science to solve business problems using real-world data. The team serves medical, market access and strategy & new product planning in the strategy, design and execution of evidence and insights, by identifying and sourcing fit-for-purpose data as well as designing evidence strategy and conducting real-world studies to deliver impact for customers, including patients, physicians, payers and regulators.  This team is at the forefront of unlocking value from real-world data and translating data into insights and evidence to better understand patient needs, change the practice of medicine, inform regulatory and access decision-making and ultimately improve health outcomes.

Main responsibilities:

As a member of the Eurasia Medical Team and contributor to the medical evidence generation community, the Data Generation & Scientific Communication Manager Eurasia builds on training and experience in health sciences and epidemiology research, public health, and regulations to ensure that relevant medical evidence is available and strategically used to contribute in the development, launch and commercialization of drugs throughout the entire product lifecycle, in the designated TA scope.

Data generation:

• Be the local medical RWE expert and central connection with global RWE experts to ensure excellence in execution on brand RWE strategies, especially for pre-launch periods and launch brands, data strategies and RWE transformational initiatives.
• Develop and implement strategies for the identification, collection, evaluation, and analysis of real-world data (RWD) sources in the Eurasia /country, to contribute on various research initiatives and business objectives at Eurasia level, aligned with global brand and RWE strategies.
• Design and oversee observational studies, registries, and other real-world evidence-generating activities, including retrospective analysis of existing databases, ensuring compliance with regulatory requirements and ethical standards.
• Identify and evaluate local data gaps and opportunities in partnership with the global RW Data Strategy & Partnership Lead and Evidence Strategy Leads, that is fit-for-purpose to identified evidence gaps from brand IEGPs and the RWE data strategy.
• Manage relationships with external vendors, including contract research organizations (CROs), data providers, and academic institutions, to facilitate data acquisition, processing and analysis.
• Collaborate cross-functionally with internal stakeholders including clinical research units, medical affairs, market access, and commercial teams to identify research questions and generate evidence-based insights.
• Lead the analysis and interpretation of real-world data, employing advanced statistical methods and epidemiological techniques to derive meaningful insights, in collaboration with internal and external experts.
• Participating in external scientific engagement and maintaining at Eurasia level, to facilitate the collection of insights, challenges and best practices, as well as to deliver opportunities to shape the external acceptability of RWE.
• Prepare and present findings from real-world evidence studies to internal and external stakeholders, including scientific conferences, ministries of health, regulatory agencies, and healthcare providers.
• Lead the local upskilling of RWE with global initiatives, events and learning opportunities, coordinated with the global upskilling in RWE strategic initiative. Create and organize local activities to enhance learner motivation and deliver an effective learning experience.
• Stay abreast of developments in real-world evidence methodologies, advances in data science, regulatory guidance, and healthcare data trends, and integrate relevant insights into project planning and execution.
• Contribute to the development of real-world evidence strategies relevant to the Eurasia and integrated evidence generation plans to support product development, regulatory submissions, and market access efforts.
• Represent global RWE in country medical leadership team to facilitate seamless communication, coordinate, and alignment of RWE with medical strategies and changing business needs.
• Provide guidance and support to cross-functional teams on the use and interpretation of real-world evidence in decision-making processes.
• Drive the timely execution of the RWE operational plan

Scientific communication:

• Be the local scientific communication expert to ensure excellence in execution in Scientific communication strategy for related therapeutic areas and brands
• Develop, implement, and execute scientific communication strategy at Eurasia level to reach therapeutic areas and brand related goals, aligned with global brand strategies
• Design scientific communication plan at Eurasia level with alignment with global one
• Ensure in operational process for scientific communication, including scientific articles, posters, etc, is in place according to company policies, politics and procedures, industry standards and legislation
• Ensure in timely execution of scientific communication plan

Alignment/Leadership:

• Facilitate collaboration with internal and external stakeholders interacting with the country medical teams to achieve data generation and scientific communication goals.
• Be point of contact for the Medical Operations Lead Eurasia to facilitate the adherence of local teams to global processes.
• Manage and enforce alignment with global policies and ensures data generation and scientific communication activities are implemented with respect of the highest ethical standards both corporate and industry. 

Transversal projects

• Contribute or facilitate (as appropriate) the implementation at Eurasia /local level of the internal projects intended to simplify and optimize the medical transformation processes and resources. Coordinates project activities, when appropriate, within his/her country and Eurasia, to allow optimal progress in decision-making.
• Contribute to external activities to shape legislation environment
• Enhance performance & ensure continuous process improvement and simplification for the benefit of business objectives related to medical activities

Foster a culture of evidence-based decision-making by promoting the value of real-world data and evidence within the organization and with external stakeholders, work on the development of local databases if relevant

About you

Education:

• Advanced degree in life sciences, epidemiology, biostatistics, data science or equivalent discipline
• Post-graduate education in business or management is preferable
• Academic degree is preferable

Work experience:

• Minimum of 2 years in Real World Data (RWD) studies management
• Experience in application of RWD studies in the Research & Development and/or commercial activities of the Company
• Minimum of 2 years in coordination of cross-functional team(s)

Key Qualifications and Competencies:

• Expertise in data generation and scientific communication strategy building and execution
• Deep understanding of procedural and operational points of RWD management and scientific communication
• Knowledge of development trends in pharmaceutical industry and principles of drug clinical study development; understanding of the goals and needs for Real World Evidence (RWE)
• Deep understanding of the regulatory/payer environment including legislation and reimbursement activities
• End-to-end leadership of RWE studies from concept to study completion and publication for regulatory or reimbursement submissions
• Analysis of data needs and/or data sources for a disease area or pharmaceutical product
• Proven experience in the field of clinical/epidemiology/public health with expertise in developing epidemiological studies
• Demonstrated experience in strategic evidence generation
• Significant peer reviewed publication track record in epidemiology, clinical and statistical and/or HEOR journals required
• Experience working in multiple therapeutic areas: transplant, type 1/2 diabetes or cardiovascular, Immunology, Rare Diseases and/or Hematology highly preferred.
• Demonstrated network collaboration experience, including with complex global matrix teams

Languages:

• Fluent in English, written and oral communication

Soft skills:

• Ability to effectively cooperate cross-functionally as a strong team player
• Excellent written and oral communication skills: ability to influence and negotiate positively and constructively
• Attention to details 
• Collaborative, able to manage stakeholder relationships at glocal level
• Apply growth mindset to develop new skills or knowledge
• Demonstrated strong strategic thinking and strategic approach to problem-solving.
• Systematic thinking and focus on impact
• Strong sense of urgency, ownership and proactive attitude to deliver value to our brands

Technical skills: 

• Expert knowledge in RWE, pharmaco-epidemiology, health outcomes research or data science
• Ability to build an evidence strategy from business needs and translate into study requirements
• Demonstrated ability to critically assess data, methods and study designs, and relate those aspects to evolving product strategy
• End-to-end project management of real-world studies and management reporting
• Proficiency in evaluating data sources to determine fit-for-purpose
• Good working knowledge of the commercial strategy (i.e. market share, competitors, product positioning) and ability to adapt evidence strategy in anticipation of market changes
• Strong portfolio management skills to manage multiple concurrent projects

We do not stop there, Explore:

Hybrid Working Options (for Istanbul HQ and for eligible white collar positions at M&S site)    

Comprehensive Medical Plan

Company Private Pension Plan  

Flexible Benefits Program for YOU to design your benefits

Company car for eligible positions & attractive lunch voucher/cafeteria at M&S site

Birthday Leave to celebrate YOU

14-week Parental Leave

Employee Stock Purchase Plan dedicated to Sanofians

Kindergarten Allowance for female employees

Employee Assistance Program

Access to various learning & development resources, career development opportunities

& MORE!

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!