Senior Clinical Data Scientist

Boehringer Ingelheim; Ridgefield (CT); Remote; USD 100,000 - 140,000; Full time

Job summary

A leading company in pharmaceuticals is seeking a Senior Clinical Data Scientist to manage phase I-IV clinical trials and contribute to innovative data analysis solutions. This position requires a strong background in statistics and data science, as well as experience with clinical data. The role offers the opportunity to make significant contributions to clinical development while promoting health and well-being through impactful projects.

Benefits

Employee referral program benefits

Health and wellness programs

Qualifications

• 3 years experience with a Master's degree OR 5 years with a Bachelor's degree.
• Experience with statistical concepts and clinical trials.
• Experience using software languages including SAS, R, or Python.

Responsibilities

• Transform, analyze, and report phase I-IV clinical trials.
• Ensure adherence to GxP requirements and department guidelines.
• Solve complex problems in clinical research and development.

Skills

Statistical methodology

Data Science

Basic medical terminology

Education

Master's degree in Statistics, Applied Mathematics, Computer Science, or related field

Bachelor's degree in Statistics, Applied Mathematics, Computer Science, or related field

Tools

SAS

R

Python

Job description

Join to apply for the Senior Clinical Data Scientist role at Boehringer Ingelheim

Join to apply for the Senior Clinical Data Scientist role at Boehringer Ingelheim

Description

POSITION ELIGIBLE FOR BENEFITS UNDER EMPLOYEE REFERRAL PROGRAM

Description

POSITION ELIGIBLE FOR BENEFITS UNDER EMPLOYEE REFERRAL PROGRAM

Employer: Boehringer Ingelheim Pharmaceuticals, Inc.

Job Title: Senior Clinical Data Scientist

Location: 900 Ridgebury Road, Ridgefield, CT 06877 (Telecommuting permitted: work may be performed in any location in the U.S.)

Job Duties: Accountable for transforming, analyzing and reporting phase I-IV clinical trials and support complex phase I-IV clinical trials or projects with established BI experience. Accountable for 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 and in particular new transformation and analysis solutions and innovative processes/tools within and outside BI. Present compelling validated stories regarding data science aspects to Biostatistics and Data Sciences (BDS) colleagues and colleagues within and outside BI with basic knowledge in data science. Ensure data transformation and analysis specifications to ensure completeness, correctness and adherence to department guidelines and SOPs as well as to applicable GxP requirements. Support other colleagues, internal and external customers, and external providers on data science related tasks. Participate in cross-functional human pharma internal working-groups or lead cross-functional BDS internal working-groups and drive/plan relevant data science aspects. Ensure cross-functional and team-based working within BDS and with neighboring units at BI. Know, understand, and implement: (i) international regulations and guidelines for good clinical and statistical practice from all International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) regions, (ii) the various international guidelines on clinical development, including statistical methodology, for Therapeutic Area (TA)-related disease areas, and (iii) BI processes and SOPs that govern clinical development in particular with respect to strategic areas (e.g., Clinical Development Plan). Solve complex, defined problems with operational / limited strategical impact within clinical research and development, taking into account needs and requirements of other units and departments. Interact with various other functions and roles within and outside BDS contributing to and/or having operational impact regarding substance level, including colleagues from Global Clinical Operations (GCO), Global Pharmacovigilance (GPV), TAs, Translational Medicine and Clinical Pharmacology (TMCP), and Global Regulatory Affairs (GRA). Represent BI for regulatory issues and requests around planning, analyses and data transformation regarding the trial/project/asset. *Telecommuting permitted: work may be performed in any location in the U.S.

Work Schedule: 40 hours per week (8:00am to 5:00pm)

Description (cont'd)

Job Requirements: Master's degree (U.S. or foreign equivalent) in Statistics, Applied Mathematics, Computer Science, or related field and three (3) years of experience in the job offered or in a related role OR Bachelor's degree (U.S. or foreign equivalent) in Statistics, Applied Mathematics, Computer Science, or related field and five (5) years of experience in the job offered or in a related role. Must have experience with: statistical methodology, design of clinical trials or clinical experiments, basic medical terminology, and processing of clinical trial information; advanced statistical concepts related to Data Science, including regression analysis, survival analysis, multivariate analysis, and hypothesis testing; using software language, including SAS, R, or Python; leading and facilitating meetings; working in global and remote teams; identifying, as well as interacting with internal and external stakeholders on, routine data science issues and solutions; and, working with the pharmaceutical industry, Contract Research Organizations, regulatory authorities, or academic institutions. 20% domestic and international travel required.

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 \u2013 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 \u2013 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

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Pharmaceutical Manufacturing

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