Boehringer Ingelheim
AD, Principal / Sr AD, Sr Principal Clinical Data Scientist
Boehringer Ingelheim, Ridgefield, Connecticut, us, 06877
AD, Principal / Sr AD, Sr Principal Clinical Data Scientist
Join to apply for the
AD, Principal / Sr AD, Sr Principal Clinical Data Scientist
role at
Boehringer Ingelheim
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 such as actual trial data, registries and real‑world databases. In particular this includes the provision of analytics tools, outputs and inference as necessary for the specific use case. You may act as a BDS product owner up to Therapeutic Area/asset level and 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 patients and customers. Our global presence provides opportunities for all employees to collaborate internationally, offering visibility and the chance to directly contribute to the company’s success. We support our employees through a healthy work environment, meaningful work, mobility, networking and work‑life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our people.
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 the design, transformation, analysis and reporting of other data from research and development such as registries and real‑world databases for specific use cases or projects/assets.
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 meet completeness, correctness, department guidelines, SOPs and applicable GxP requirements.
Guide and/or lead other colleagues, internal and external customers and 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, support the clinical drug development process as a BDS Product Owner up to the level of substance/assets.
Ensure cross‑functional and team‑based working within BDS and with other units at BI, fulfilling tasks of other functions as needed and contributing to cross‑functional 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, transforming, analyzing and reporting complex phase I‑IV clinical trials that present new challenges and lack given project and therapeutic knowledge, such as mega trials or new indications and 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 and other professionals within and outside of BI.
Ensure data transformation and analysis specifications to meet completeness, correctness, department guidelines, SOPs and applicable GxP requirements.
Lead/Guide other colleagues, internal and external customers and 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, support the clinical drug development process as a BDS Product Owner up to the level of Therapeutic Area/assets.
Facilitate and ensure cross‑functional and team‑based working within BDS and with the rest of the company, fulfilling tasks of other functions as needed and contributing to cross‑functional thinking.
Foster innovative digital approaches to produce sophisticated, intelligent optimization solutions, innovative processes and predictive models.
Requirements AD Requirements
Bachelor of Science (BSc) in Statistics, Mathematics, Computer Science or related field with a minimum of seven (7) years of data science experience; or
Master of Science (MSc) in Statistics, Mathematics, Computer Science or related field with six (6) years of experience within the pharmaceutical industry, CROs, regulatory authorities or academic institutions; or
Doctoral Degree (PhD) in Statistics, Mathematics, Computer Science or related field 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 application of key 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 and projects.
Thorough knowledge of statistical methodology, design of clinical trials or clinical experiments, basic medical terminology and processing clinical trial information.
Advanced working knowledge of a broad variety of relevant software languages.
Mindful of local, global, internal and external cultures to ensure 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 in a 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).
Knowledge of: International regulations and guidelines for good clinical and statistical practice from all ICH regions; 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) with a minimum of ten (10) years of data science experience; or
Master of Science (MSc) with ten (10) years of experience within the pharmaceutical industry, CROs, regulatory authorities or academic institutions; or
Doctoral Degree (PhD) 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 other compensation elements. For an overview of our benefits please click here.
Why Boehringer Ingelheim? With us, you can develop your own path in a company with a culture that values our differences and drives innovation. Your development is our priority, with programs and groups that support health, wellbeing and global accessibility to healthcare. By being part of a constantly innovating team, you’ll help transform lives for generations.
Seniority level Mid‑Senior level
Employment type Full‑time
Job function Engineering and Information Technology
Industries Pharmaceutical Manufacturing
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AD, Principal / Sr AD, Sr Principal Clinical Data Scientist
role at
Boehringer Ingelheim
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 such as actual trial data, registries and real‑world databases. In particular this includes the provision of analytics tools, outputs and inference as necessary for the specific use case. You may act as a BDS product owner up to Therapeutic Area/asset level and 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 patients and customers. Our global presence provides opportunities for all employees to collaborate internationally, offering visibility and the chance to directly contribute to the company’s success. We support our employees through a healthy work environment, meaningful work, mobility, networking and work‑life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our people.
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 the design, transformation, analysis and reporting of other data from research and development such as registries and real‑world databases for specific use cases or projects/assets.
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 meet completeness, correctness, department guidelines, SOPs and applicable GxP requirements.
Guide and/or lead other colleagues, internal and external customers and 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, support the clinical drug development process as a BDS Product Owner up to the level of substance/assets.
Ensure cross‑functional and team‑based working within BDS and with other units at BI, fulfilling tasks of other functions as needed and contributing to cross‑functional 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, transforming, analyzing and reporting complex phase I‑IV clinical trials that present new challenges and lack given project and therapeutic knowledge, such as mega trials or new indications and 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 and other professionals within and outside of BI.
Ensure data transformation and analysis specifications to meet completeness, correctness, department guidelines, SOPs and applicable GxP requirements.
Lead/Guide other colleagues, internal and external customers and 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, support the clinical drug development process as a BDS Product Owner up to the level of Therapeutic Area/assets.
Facilitate and ensure cross‑functional and team‑based working within BDS and with the rest of the company, fulfilling tasks of other functions as needed and contributing to cross‑functional thinking.
Foster innovative digital approaches to produce sophisticated, intelligent optimization solutions, innovative processes and predictive models.
Requirements AD Requirements
Bachelor of Science (BSc) in Statistics, Mathematics, Computer Science or related field with a minimum of seven (7) years of data science experience; or
Master of Science (MSc) in Statistics, Mathematics, Computer Science or related field with six (6) years of experience within the pharmaceutical industry, CROs, regulatory authorities or academic institutions; or
Doctoral Degree (PhD) in Statistics, Mathematics, Computer Science or related field 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 application of key 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 and projects.
Thorough knowledge of statistical methodology, design of clinical trials or clinical experiments, basic medical terminology and processing clinical trial information.
Advanced working knowledge of a broad variety of relevant software languages.
Mindful of local, global, internal and external cultures to ensure 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 in a 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).
Knowledge of: International regulations and guidelines for good clinical and statistical practice from all ICH regions; 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) with a minimum of ten (10) years of data science experience; or
Master of Science (MSc) with ten (10) years of experience within the pharmaceutical industry, CROs, regulatory authorities or academic institutions; or
Doctoral Degree (PhD) 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 other compensation elements. For an overview of our benefits please click here.
Why Boehringer Ingelheim? With us, you can develop your own path in a company with a culture that values our differences and drives innovation. Your development is our priority, with programs and groups that support health, wellbeing and global accessibility to healthcare. By being part of a constantly innovating team, you’ll help transform lives for generations.
Seniority level Mid‑Senior level
Employment type Full‑time
Job function Engineering and Information Technology
Industries Pharmaceutical Manufacturing
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