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　　Job Description

　　Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as a Data Configuration Engineer in our Cambridge, MA office.

　　At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

　　Here, you will be a vital contributor to our inspiring, bold mission

　　OBJECTIVES:

　　The Clinical Data Sciences group is responsible for integrating structured and unstructured data across the various data sources, setup, data transfer/review and support downstream transformation and analysis.

　　The Clinical Data Sciences comprises of the Clinical Data Engineering and Clinical Data Standards. While the Clinical Data Standards provides the standards for clinical operation and data flow, the Clinical Data Engineering team drives the data architecture for clinical data. CDS also provides support to exploratory and specialty data for the purposes of data modelling, simulation, and analysis.

　　Key to Takeda’s success is the Clinical Data Engineering team, provides strategic planning, integrating, execution, build and oversight of clinical trial deliverables. CDCS leads the integration of collected data from all sources by setting up proper configuration of data extraction and mapping of raw data into the Common Data Model for individual studies using processes and by the Data Engineer. Work with Data Engineer to configure (Extract Transform Load) ETLs and (Extract Load and Transform) ELTs. Provide testing and documentation for data pipelines. Utilize and contribute to libraries for functions and transformation templates for reuse for study level configuration tasks.

　　The Data Configuration Engineer (DCE), configures and maintains the data pipelines that conform to the common data model that ensures data ingestion for all study-level data capture technologies and other related vendor and/or applications (e.g., EDC, IRT, ePRO, eCOA). Liaise cross functionally, and provides oversight that facilitates test data transfer, and confirms accurate DTA specification. Performs tasks to, configure, maintain, and monitor data flow integration between collected data and the clinical data repository (CDR). DCE contributes to the successful conduct of Takeda’s clinical trials and to the delivery of high quality in a timely manner, which is eventually used for statistical analysis and submitted to regulatory authorities for the approval of Takeda products. Further, CDCS efforts enable valid secondary use of clinical trial data throughout Takeda research groups to maximize value and achieve company objectives.

　　ACCOUNTABILITIES:

　　Advanced knowledge and ability to liaise with outside groups in a matrix environment

　　Thorough understanding of industry standards and ways of working

　　Understand FDA requirements and ability to defend work in audit

　　Ability to mentor and train other team members

　　Configure data extraction and transformations in an individual contributor role across multiple data sources at the study level as defined by the Data Transfer Agreement and other specifications provided by Data Engineer

　　Partner closely with internal/external stakeholders and data engineers in a collaborative manner

　　Ensure accurate delivery of data format and data frequency with quality deliverables per specification

　　Participate in the development, maintenance and training rendered by standards and other functions on transfer specs and best practices used by business

　　Additional Activities:

　　Provide input for SOP creation

　　Assists with quality review of above activities performed by a vendor, as needed.

　　Adhere to SOPs for computer system validation and all GCP (Good Clinical Practice) regulations.

　　Ensure compliance with own Learning Curricula, corporate and/or GxP requirements. Performs other duties as assigned within timelines

　　EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:

　　Education

　　Bachelor's degree plus minimum of 5+ years’ experience (Manager in computer science, statistics, biostatistics, mathematics, biology or other health related field or equivalent experience that provides the skills and knowledge necessary to perform the job.Experience

　　Experience with EDC build, Data Management, and EDC extraction configuration

　　Knowledge of data flow between clinical data management systems, vendor devices and CDR.

　　Knowledge of XMLS, ALS, APIs and MDR preferred.

　　Experience with one of these languages: SQL, SAS, R, Python preferred.

　　Understanding of SDTM

　　Strong working knowledge of clinical trial terminology and data transfer specification

　　Proven ability to resolve problems independently and collaboratively.

　　Must be able to work in a fast-paced environment with demonstrated ability to juggle and prioritize multiple competing tasks and demands.

　　Ability to work independently, take initiative and complete tasks to deadlines.

　　Special Skills/Abilities:

　　Strong attention to detail, and organizational skills

　　Good time management skills

　　Quick learner and comfortable asking questions, learning new technologies and systems

　　Good knowledge of office software (Microsoft Office).

　　Experience with EDC build or data extraction configuration ETL/ELT experience

　　Understanding of AWS/Data bricks concepts

　　Preferable but not required:

　　Experience developing R shiny and Python apps

　　Experience with Agile development methods

　　Experience with Veeva CDB

　　License/Certifications:

　　Preferred to have SAS or R or Python certificationLocation and Salary Information:

　　This position is currently classified as “remote” in accordance with Takeda’s Hybrid and Remote Work policy.

　　Base Salary Range: $91,700 to $131,000, based on candidate professional experience level. Employees may also be eligible for Short Term and Long-Term Incentive benefits as well. Employees are eligible to participate in Medical, Dental, Vision, Life Insurance, 401(k), Charitable Contribution Match, Holidays, Personal Days & Vacation, Tuition Reimbursement Program and Paid Volunteer Time Off.

　　WHAT TAKEDA CAN OFFER YOU:

　　401(k) with company match and Annual Retirement Contribution Plan

　　Tuition reimbursement

　　Company match of charitable contributions

　　Health & Wellness programs including onsite flu shots and health screenings

　　Generous time off for vacation and the option to purchase additional vacation days

　　Community Outreach Programs

　　Empowering Our People to Shine

　　Learn more at takedajobs.com .

　　No Phone Calls or Recruiters Please.

　　#LI-JV2

　　EEO Statement

　　Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

　　Locations

　　Massachusetts - Virtual

　　Worker Type

　　Employee

　　Worker Sub-Type

　　Regular

　　Time Type

　　Full time

　　#LI-Remote