AD, Principal / Sr AD, Sr Principal Clinical Data Scientist

Description

As a Principal / Sr Principal Clinical Data Scientist, you would support the clinical drug research and development process by providing strategic planning and execution, including data transformation and all aspects of descriptive, diagnostic, predictive and prescriptive analytics of data related to clinical projects like actual trial data, registries and real-world data bases. In particular this includes the provision of analytics tools, outputs and inference as necessary for the specific use case. May act as a BDS product owner up to Therapeutic Area/asset level. Represent BDS at a substance/asset level regarding data science related aspects.

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.

Duties & Responsibilities

AD Responsibilities:

• Lead and oversee designing, transforming, analyzing and reporting complex phase I-IV clinical trials or projects with established BI experience and supporting complex international R&D projects.
• Lead and oversee for designing, transforming, analyzing and reporting of other data from research and development like registries and real-world data bases with respect to a specific use case or project/asset.
• Keep abreast of data science within and outside BI. Turn derived insights into new data science approaches relevant for clinical development, registration, and marketing of drugs.
• Present compelling validated stories regarding complex data science aspects to BDS colleagues and other professionals within and outside of BI.
• Ensure data transformation and analysis specifications to ensure completeness, correctness and adherence to department guidelines and SOPs as well as to applicable GxP requirements.
• Guide and/or lead other colleagues, internal and external customer and external providers on data science related tasks.
• Participate in cross-functional BI internal working-groups or lead cross-functional human pharma internal working-groups and drive/plan relevant data science aspects. Participate in external working groups.
• If applicable, supports the clinical drug development process as a BDS Product Owner up to the level of substance/assets.
• Ensures cross-functional and team-based working within BDS and with other units at BI. Fulfils tasks of other functions as needed and possible. Contributes to cross-functional- and team-based thinking.
• Support fostering innovative digital approaches to produce sophisticated, intelligent optimization solutions, innovative processes and predictive models.
  
  
  

Sr AD Responsibilities:

• Subject Matter Expert (SME) / Process Lead for designing as well as transforming, analyzing and reporting complex phase I-IV clinical trials that represent new challenges and for which project and therapeutic knowledge is not given, such as mega trials or new indications and for complex international R&D projects.
• Identify trends in data science within and outside BI . Initiate and turn derived insights into new data science approaches relevant for clinical development, registration, and marketing of drugs.
• Present compelling validated stories regarding complex data science aspects to BDS colleagues, other professionals within and outside of BI.
• Ensure data transformation and analysis specifications to ensure completeness, correctness and adherence to department guidelines and SOPs as well as to applicable GxP requirements.
• Lead/Guide other colleagues, internal and external customer and external providers on data science related tasks.
• Lead cross-functional BI internal working-groups and drive/plan relevant data science aspects. Participate in external working groups.
• If applicable, supports the clinical drug development process as a BDS Product Owner up to the level of Therapeutic Area/assets.
• Facilitates and ensures cross-functional and team-based working within BDS and with the rest of the company. Fulfils tasks of other functions as needed and possible. Contributes to cross-functional- and team-based thinking.
• Fosters innovative digital approaches to produce sophisticated, intelligent optimization solutions, innovative processes and predictive models.
  
  
  

Requirements

AD Requirements:

• Bachelor of Science (BSc) from an accredited institution in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc.), with a minimum seven (7) years of data science experience; Or
• Master of Science (MSc) from an accredited institution in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc.), with six (6) years of experience within the pharmaceutical industry, CROs, regulatory authorities or academic institutions; Or
• Doctoral Degree (PhD) from an accredited institution in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc.), with three (3) years of experience within the pharmaceutical industry, CROs, regulatory authorities or academic institutions
• Working experience might be partially compensated by broad and deep topic-specific knowledge
• Broad knowledge and advanced experience in software languages relevant for business needs
• Broad knowledge and advanced experience in understanding of clinical trial development process required
• Advanced project lead experience required
• Understanding and applying key of principles of data science
• In-depth understanding of advanced statistical concepts related to Data Science
• Demonstrated broad knowledge in planning, transforming, analyzing, interpreting, and reporting data in complex clinical trials, in projects with established BI experience or data from other sources in clinical research and development
• Thorough knowledge of statistical methodology, design of clinical trials or clinical experiments, basic medical terminology and on processing clinical trial information
• Advanced working knowledge of broad variety of aspects of relevant software languages
• Mindful of local, global, internal and external cultures to ensure that messages are received positively and effectively
• Ability to lead and facilitate meetings
• Ability to develop and deliver training related to data science topics
• Evidence of strong teamwork, also in global and remote context
• Good interpersonal skills with the ability to interact effectively with people, internally and externally (e.g. CROs, experts, management)
• Ability to pro-actively identify issues and solutions and to interact with internal and external bodies on routine data science issues
• Language skills: English: fluent (Read/Write/Speak)
• Know, understand, and implement:
• International regulations and guidelines for good clinical and statistical practice from all ICH regions,
• The various international guidelines on clinical development, including statistical methodology, for TA-related disease areas, and
• BI processes and SOPs that govern clinical development in particular with respect to strategic areas (e.g. Clinical Development Plan)
  
  
  

SR AD Requirements

• Bachelor of Science (BSc) from an accredited institution in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc.), with a minimum of ten (10) years of data science experience; Or
• Master of Science (MSc) from an accredited institution in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc.), with ten (10) years of experience within the pharmaceutical industry, CROs, regulatory authorities or academic institutions; Or
• Doctoral Degree (PhD) from an accredited institution in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc.), with six (6) years of experience within the pharmaceutical industry, CROs, regulatory authorities or academic institutions.
  
  
  

Compensation

This position offers a base salary typically between $140,000 and $222,000 for AD level and $170,000 and $269,000 for Sr AD level. The position may be eligible for a role specific variable or performance based bonus and or other compensation elements.  For an overview of our benefits please click here .

Our Company

Why Boehringer Ingelheim?

With us, you can develop your own path in a company with a culture that knows our differences are our strengths - and break new ground in the drive to make millions of lives better.

Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.

Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after - as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations.

Want to learn more? Visit https://www.boehringer-ingelheim.com