Medical - Real-World Evidence Data Scientist Job at Sanofi-Aventis Deutschland GmbH (Beijing)

Real-World Evidence Data Scientist

To supervise and provide inputs to data management and statistical analyses for ...

Location

China , Shanghai

Salary:

Not provided

Sanofi-Aventis Deutschland GmbH

Expiration Date

Until further notice

Requirements

Master degree in biostatistics/statistics, mathematics, epidemiology or relevant fields
At least 2 years of working experience preferable on observational real-world studies
Strong analytic skills of analyzing real-world data (including big electronic medical datasets)
Proficient in using statistical software (SAS/R/Python)
SAP writing experience
Ability to work effectively in a multi-cultural context as a good team member
Great potential/Capability to provide statistical leadership to cross-functional teams at the study level
Effective English communication skills in relating to colleagues and associates both inside and outside the organization
Ability to communicate in a credible and confident manner

Job Responsibility

Interact with CRO to supervise and provide inputs to data management and statistical analyses and ensure timeliness and quality of statistical deliverables according to agreement in assigned projects
From statistical perspectives to advise internal Medical team on study design, data management, statistical analysis, interpretation of statistical results, and publications
Perform programming and analytical activities for data cleaning and statistical deliverables in post-hoc analyses after the completion of a primary data collection study, i.e., secondary use of pre-existing medical databases
Align with stakeholders on planning, delivering and communicating statistical analyses, data presentations, scientific reports, and publications
Comply with all statistics and quality processes and standards that are applicable to statistical outputs, and support processes that require statistical input
Continuously assess the growth and accessibility of external real-world data assets, evaluate data quality and fitness-for-purpose, and develop compliant and efficient engagement models with data providers to enable robust RWE generation across TAs
Perform other duties, as assigned

New

Clinical Real World Data Scientist

The Clinical RWD Scientist is a critical role within the Data Assessment Center ...

Location

Canada , Toronto

Salary:

108900.00 - 157300.00 CAD / Year

Sanofi-Aventis Deutschland GmbH

Expiration Date

June 12, 2026

Requirements

Advanced degree (Master's or PhD) in Epidemiology, Biostatistics, Health Informatics, Health Economics, Pharmacoepidemiology, or a closely related quantitative discipline
Minimum 4-5 years for Master’s degree holder or 2-4 years for Doctoral degree holder of relevant experience in real-world data, commercial analytics, real-world evidence, health outcomes research, fit-for-purpose feasibility assessment, data quality assessment or a related field within the pharmaceutical, biotech, or health technology industry
Experience in predictive modeling using RWD to identify at risk patient populations with a publication record in peer-review journals
Experience in patient & healthcare provider segmentation to inform Medical and Commercial strategy
Demonstrated expertise in epidemiological study design and statistical methods such as propensity score matching, descriptive statistics, regression analysis, predictive modelling
Strong proficiency in statistical programming languages: SQL, Python, R, and/or SAS
Solid working knowledge of Snowflake for database querying and data extraction
Familiarity with medical coding systems: ICD-10, CPT, SNOMED CT, LOINC, RxNorm and experience/knowledge on OHDSI OMOP CDM standardized data model for healthcare data
Understanding of US EHR, claims, disease registry data, public health surveillance data as well as US healthcare billing system
Experience with AI coding tools such as Cursor, GitHub Copilot, Claude, LLM

Job Responsibility

Design and execute rigorous data assessment frameworks
Evaluating the fitness-for-purpose of real-world data (RWD) sources for insights or evidence generation across the enterprise
Support the development of reliable RWD Foundation and Products
Lead and execute feasibility assessments for RWD sources
Develop and apply structured data assessment frameworks to evaluate data quality dimensions
Assess the availability and representativeness of patient populations within RWD sources
Evaluate the feasibility of extracting structured and unstructured data elements from EHR systems
Document assessment outcomes in standardized feasibility reports and communicate findings clearly to cross-functional stakeholders
Identify and articulate limitations of RWD sources
Design methodologically sound recommendations & minimize misuse of RWD

What we offer

High-quality healthcare
Prevention and wellness programs
At least 14 weeks’ gender-neutral parental leave

Fulltime

Senior Manager, MED Oncology RWE/Epi Scientist

The Senior Manager, Oncology, position within Medical Evidence Development (MED)...

Location

United Kingdom , Walton Oaks

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

PhD in Epidemiology, Statistics/Biostatistics, Health Outcomes Research, Quantitative Methods, Public Health, Health Economics, or Other Biological Science fields with a substantial quantitative component and at least 1 years of relevant experience in the pharmaceutical, academic and/or medical environment
or, MPH or another relevant Master’s degree and at least 5 years of experience in the pharmaceutical, academic and/or medical environment, at least 1 of which were in the pharmaceutical industry
Demonstrated strong quantitative skills and methods expertise to generate rapid insights from real-world / observational data source
Demonstrated strong technical writing skills and oral presentation skills with a track-record of publishing in peer-reviewed journals and presenting at medical/scientific conferences
Demonstrated ability to convert complex analysis into meaningful insights with data visualization and presentation tools and able to manipulate and analyze complex structured and unstructured data from multiple real world evidence sources
Ability to work under pressure with a high level of autonomy/leadership on research projects and collaborate with multiple partners in a matrixed environment
Knowledgeable of the external regulatory environment for real-world evidence and maintains awareness of scientific developments in epidemiology, medicine, and technology (e.g., artificial intelligence)

Job Responsibility

Synthesizing the literature and contributing to the design, conduct and reporting of global epidemiologic research studies on Pfizer I&I products
Accountable for the quality, timeliness, and efficiency of all RWE/Epi deliverables in assigned product/disease area
Maintain an internal network of Pfizer stakeholders to cultivate innovation, cross-functional collaboration, and identify new opportunities for RWE/Epi to increase the value of Pfizer assets
Develop external partnerships to leverage data resources and collaboration on high priority global studies
Authoring and reviewing study protocols, reports, and presentations, as well as communication in writing and presentations to internal stakeholders, regulatory authorities, and medical professionals
Responsible for non-study deliverables such as RWE insights, epidemiology literature reviews, regulatory responses, and department initiatives
Identifying, designing and supporting or leading real-world evidence studies of disease epidemiology and effectiveness as part of the global cross-functional Integrated Evidence Plan
Maintain knowledge and awareness of internal and external data resources and identify appropriate studies for addressing questions of interest
Partner with Chief Medical Office colleagues to address asset team evidence needs and support global regulatory submissions to the FDA, EMA and other agencies
Deliver rapid insights from real-world, observational data source

Fulltime

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

For drugs to be successful, there must be robust health outcomes data to support...

Location

United States , Philadelphia

Salary:

204000.00 - 340000.00 USD / Year

GSK

Expiration Date

Until further notice

Requirements

MSc, or equivalent in health outcomes, health economics, epidemiology, pharmacy, health or life sciences
3+ years of experience working in the pharmaceutical industry, preferably in a multi-national company
Experience in planning and delivering individual projects, managing budgets and working within a matrix setting
A history of designing a variety of RWE studies including prospective observational studies, cross-sectional and retrospective cohort studies, chart reviews, and database analyses
Proficiency in utilizing evidence for the development of HTA submissions, reimbursement and/or medical engagements
A track record of delivering robust payer evidence and credibility to engage meaningfully with external experts and leaders in the field
Expertise with the diversity and complexity of healthcare markets, health technology assessment agencies, and reimbursement decision making globally, in region and local markets
Experience in communicating technical and complex concepts and results to various audiences to impact decision-making
Experience in oncology.

Job Responsibility

Plan, design and execute multiple studies for a given asset and manage timelines, deliverables, and budget
Assure quality of deliverables, including review and sign off project specifications, protocols, data analysis plans, final study reports, abstracts, posters and manuscripts, in adherence to SOPs
Identify resources, references and analyses to inform scientific design and advise internal experts.(medical affairs, clinical, commercial/market access) and external experts as needed in support of the asset team
Translate needs for evidence into study concepts in alignment with strategic objectives and vision for the asset, e.g. development of study protocols and proposing innovative and cost-effective ways of developing and executing studies
Develop and maintain a good working knowledge of real-world data resources, existing partnerships and public initiatives and become the point person for select sources to advise on their suitability to address given research questions
Develop a deep understanding of customers’ needs, including clinicians and HTA requirements, and their acceptance of different types of evidence and impact of that evidence to their decision making
Collaborate with internal teams and participate in best practice sharing sessions across the non-interventional study organization
Build strong working relationships with stakeholder groups across medical, market access, R&D and commercial to ensure strategic alignment and optimal cross-functional collaboration and communication
Ensure key stakeholders, including TA aligned business leaders, are regularly updated on plans through periodic reporting
Develop excellent working relationships with external thought leaders to ensure appropriate methods and research agendas are applied, in accordance with GSK policies.

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes
Health care and other insurance benefits (for employee and family)
Retirement benefits
Paid holidays
Vacation

Fulltime

Amyloidosis, Medical Affairs Scientist

The MAS role family comprises a variety of medical scientific specialties, such ...

Location

Japan , Tokyo

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Minimum requirement: 4 year university undergraduate degree AND master’s degree in life science, or Pharmacists 4-year university graduates with pharmacist license and master’s degree or above or equivalent life science research experience, or 6–year university graduates with pharmacist license, or Nurses with master’s degree or above, or Veterinarians, or Dentists, or MDs
Preferred: In addition to those who meet the minimum requirements above, the qualifications below are preferred MD (clinical experience, board certification preferred), or PhD in Life Science
Technical Skills: Medical/ pharmaceutical expert knowledge of therapeutic disease area/ products
Ability to communicate appropriately and build good relationship with internal/external stakeholders
Work effectively with teams and across functions by demonstrate Pfizer’s Values & Behaviors and the agility to learn from others
Capable of medical discussion with relevant departments and external HCPs.
A person who understands compliance and relevant laws/regulations in the pharmaceutical industry and advocates the appropriate use of the products.
Can demonstrate appropriate knowledge and understanding of internal organization structure, key stakeholders and strategies
A person who is able to quickly acquire necessary medical/ scientific knowledge and skills though self-learning
Experience: Work experience at functions of: Medical Affairs

Job Responsibility

Demonstrate medical and scientific leadership and expertise
Provide and exchange medical/ scientific information for/from medical institutions (and other related sources) in the assigned area and from stakeholders.
Drive for heightened understanding of the clinical and medical attributes of our products in order to enhance the safe and efficacious use.
Maintain the highest scientific standards during in/ external activities to provide deep medical and scientific expertise.
Contribute to the implementation of local medical strategies and life cycle clinical plans for inline and pipeline medicines / vaccines to address unmet medical needs and fill data gaps.
Make important contributions to decisions of medical strategies for assigned products, in order to ensure safe, proper, and effective use of assigned products.
Contribute to achieving the department/team goals, and/or participate in cross-organizational projects as a core member and provide guidance to deliver the results.
Play an active role in supporting members in the team/organization with the line manager to move towards its goals
Develop and execute the medical plan aligned with the medical strategy to meet unmet medical needs in the assigned product(s) and therapeutic area(s) in collaboration with office medical
Identify unmet medical needs and healthcare disparities in the assigned asset(s) and therapeutic area(s) through medical activities such as advisory board meetings and scientific exchanges with HCPs and other relevant individuals and organizations.

Fulltime

R&D Director

Flen Health is looking for a dynamic and visionary R&D Director who combines str...

Location

Belgium , Kontich

Salary:

Not provided

Flen Health GmbH

Expiration Date

Until further notice

Requirements

Ph.D. in biopharmaceutical sciences, molecular biology, or a related discipline
Extensive experience in biopharmaceutical R&D, with a strong track record in wound healing and dermatology
Demonstrated hands-on expertise in functional genomics, structural and molecular biology, computational methods, and advanced skin and wound modelling
Proven success in leading and actively participating in teams and complex research projects
Strong publication and patent record in peer-reviewed journals, with direct contributions to scientific literature
Experience in securing and managing national and international research grants, including hands-on grant writing and project execution
Proven ability to lead international research consortia, delivering impactful outcomes through both strategic oversight and direct scientific involvement
Background in topical product development, with practical experience in formulation and testing

Job Responsibility

Provide both strategic direction and active, hands-on leadership to the R&D team, personally engaging in critical research activities and mentoring scientists at all levels
Lead by example in the discovery and development of new biopharmaceutical compounds, directly contributing expertise to projects targeting wound healing and skin inflammation
Build and strengthen the scientific evidence base for existing medical device products through direct involvement in experimental design, data analysis, and publication
Integrate disease insights with advanced pre-clinical methodologies, including functional genomics, structural and molecular biology, computational approaches, and both in vitro and in silico skin and wound models- by actively participating in experimental work and troubleshooting
Foster a culture of collaboration, innovation, and continuous improvement within the team by working side-by-side with team members and encouraging open scientific dialogue
Maintain a relentless focus on delivering value to patients and healthcare professionals ensuring that leadership decisions are grounded in practical, real-world impact
Establish and expand national and international research networks, leading projects and consortia that result in commercially viable innovative patents and products, including those supported by scientific grant programs

What we offer

Excellent working conditions
An innovative and inspiring work environment
Independent project work & responsibilities within a professional team
Career prospect
Learning and development opportunities
Flexible working ecosystem
Enthusiastic colleagues
Attractive remuneration package

Fulltime

R&D Director

We are looking for a dynamic and visionary R&D Director who combines strategic l...

Location

Belgium , Kontich

Salary:

Not provided

Flen Health GmbH

Expiration Date

Until further notice

Requirements

Ph.D. in biopharmaceutical sciences, molecular biology, or a related discipline
Extensive experience in biopharmaceutical R&D, with a strong track record in wound healing and dermatology
Demonstrated hands-on expertise in functional genomics, structural and molecular biology, computational methods, and advanced skin and wound modelling
Proven success in leading and actively participating in teams and complex research projects
Strong publication and patent record in peer-reviewed journals, with direct contributions to scientific literature
Experience in securing and managing national and international research grants, including hands-on grant writing and project execution
Proven ability to lead international research consortia, delivering impactful outcomes through both strategic oversight and direct scientific involvement
Background in topical product development, with practical experience in formulation and testing

Job Responsibility

Provide both strategic direction and active, hands-on leadership to the R&D team, personally engaging in critical research activities and mentoring scientists at all levels
Lead by example in the discovery and development of new biopharmaceutical compounds, directly contributing expertise to projects targeting wound healing and skin inflammation
Build and strengthen the scientific evidence base for existing medical device products through direct involvement in experimental design, data analysis, and publication
Integrate disease insights with advanced pre-clinical methodologies, including functional genomics, structural and molecular biology, computational approaches, and both in vitro and in silico skin and wound models- by actively participating in experimental work and troubleshooting
Foster a culture of collaboration, innovation, and continuous improvement within the team by working side-by-side with team members and encouraging open scientific dialogue
Maintain a relentless focus on delivering value to patients and healthcare professionals ensuring that leadership decisions are grounded in practical, real-world impact
Establish and expand national and international research networks, leading projects and consortia that result in commercially viable innovative patents and products, including those supported by scientific grant programs

What we offer

Excellent working conditions
An innovative and inspiring work environment
Independent project work & responsibilities within a professional team
Career prospect
Learning and development opportunities
Flexible working ecosystem
Enthusiastic colleagues
Attractive remuneration package

Fulltime

Senior Director, Vaccines Medical Affairs Lead

Provide scientific leadership for the vaccine business in Japan. Develop and exe...

Location

Japan , Tokyo

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Advanced degree (MD, PharmD, PhD)
10+ years of Medical Affairs experience in vaccines/infectious diseases, including 7+ years of people leadership
Proven track record in national-level strategy development and execution for new product launches/indication expansions
Experience in scientific dialogue with PMDA, MHLW, municipalities, and academic societies (presentations, chairing, committee participation)
Practical understanding of Pharmaceutical Affairs Law, GCP, GPSP, GVP, Clinical Research Law, Personal Information Protection Law, JPMA Code
Deep expertise in vaccine-related Medical Affairs
Leadership: Inspire, develop, and lead teams in dynamic environments with scientific excellence
Communication and relationship-building skills across internal and external stakeholders
Compliance: Promote appropriate use through understanding of industry regulations
Learning agility: Ability to quickly self-learn necessary medical/scientific knowledge

Job Responsibility

Develop annual Medical Affairs Plans (MAPs) aligned with Japan’s infectious disease epidemiology, NIP (National Immunization Program), local implementation, and decision-making processes
Lead launch preparation and execution for new products, indications, and technologies
Identify unmet medical needs and healthcare disparities via advisory boards
create and drive action plans to address data gaps
Lead unbiased scientific communication, HCP education seminars, data generation initiatives, and development of scientific materials
Contribute to lifecycle planning for both inline and pipeline vaccines
Design Japan Evidence Plans covering epidemiology, outcomes, and implementation science
Utilize databases (JMDC/MDV/NDB) and regional cohorts to visualize effectiveness, safety, and real-world implementation
Oversee publication and conference presentation plans
Support investigator-initiated studies and medical grants per internal policy

Fulltime

Medical - Real-World Evidence Data Scientist

Sanofi-Aventis Deutschland GmbH

Location:
China , Beijing

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 13, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Medical - Real-World Evidence Data Scientist

Real-World Evidence Data Scientist

Clinical Real World Data Scientist

Senior Manager, MED Oncology RWE/Epi Scientist

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

Amyloidosis, Medical Affairs Scientist

R&D Director

R&D Director

Senior Director, Vaccines Medical Affairs Lead

Medical - Real-World Evidence Data Scientist

Sanofi-Aventis Deutschland GmbH

Location:China , Beijing

Category:IT - Software Development

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:March 13, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Medical - Real-World Evidence Data Scientist

Real-World Evidence Data Scientist

Clinical Real World Data Scientist

Senior Manager, MED Oncology RWE/Epi Scientist

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

Amyloidosis, Medical Affairs Scientist

R&D Director

R&D Director

Senior Director, Vaccines Medical Affairs Lead

Location:
China , Beijing

Category:
IT - Software Development

Contract Type:
Not provided

Job Posted:
March 13, 2026