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Clinical Data Engineer (Manager/Sr. Manager) - Alta Petens - REMOTE

Employer
Takeda
Location
Boston, Massachusetts
Start date
Feb 1, 2023

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Discipline
Clinical, Clinical Data, Clinical Research
Required Education
Bachelors Degree
Position Type
Full time
Hotbed
Genetown, Best Places to Work

Job Details

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

Clinical Data Sciences (CDS) at Takeda:

Key to Takeda’s success the Clinical Data Sciences team provides strategic planning, integrating, execution, build and oversight of clinical trial deliverables. 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.

Clinical Data Engineer (CDE), Clinical Data Sciences (CDS):

Key to Takeda’s success is the Clinical Data Engineering team, provides strategic planning, integrating, execution, build and oversight of clinical trial deliverables. CDE leads the integration, design, development, and execution of data pipelines for the ingestion of clinical data from all sources at an enterprise level for use by the clinical data configuration specialist at the study level. The CDE is an enterprise level role and is primarily responsible for ensuring smooth end to end processes for data collection/ingestion from all data collection sources, providing an output into a data lake that is fit for use by downstream end users. The CDE is also responsible for developing and tracking KPIs and other measures across the business and providing continuous improvement for both process and tools. The CDE will also develop and maintain libraries, tools, and reports to increase reuse and overall efficiency for study level roles. The CDE should have a strong understanding of end-to-end clinical data collection and extraction processes as well as strong project management and technical experience. The CDE will be working with cross functional stakeholders to ensure alignment on processes and requirements and often will be required to convert these requirements to technical specifications. The CDE may also need to develop tools and visualizations as part of the continuous improvement process.

Under the guidance of Clinical Data Sciences, the Clinical Data Engineer provides leadership and guidance at the enterprise level for end-to-end data extraction, transformations and construct of data pipelines that conform to the common data model that ensures data ingestion for all clinical data capture technologies and other related vendor and/or applications (e.g., EDC, IRT, ePRO, eCOA) as well other data models that may be required by end users. Understands and ensures proper data formats for all downstream users for use in the data lake. Facilitates test data transfer to staging instance and confirms accurate DTA specification. Defines processes and develop and maintain code libraries for use by clinical data configuration specialist to build, maintain, and monitor data pipelines for clinical data and the clinical data repository (CDR) alongside processing specialty data for exploratory analysis.

Develops and maintains library of reusable mapping and transformation functions to be used across studies. CDE 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. The CDE also monitors end to end performance and KPIs and provides continuous improvement to processes and tools. Further, CDE efforts enable valid secondary use of clinical trial data throughout Takeda research groups to maximize value and achieve company objectives.

Key Accountabilities:

  • Experience building data pipelines for various heterogenous data sources

  • Identifying, designing, and implementing scalable data delivery pipelines and automating manual processes

  • Building required infrastructure for optimal data extraction, transformation and loading of data using cloud technologies like AWS, Azure etc.

  • Develop end to end processes on the enterprise level for use by the clinical data configuration specialist to prepare data extraction and transformations of raw data quickly and efficiently from various sources at the study level

  • Coordinate with downstream users such as statistical programmers, SDTM programming, analytics, and clinical data programmers to ensure that outputs meet requirements of end users

  • Experience creating ELT and ETL to ingest data into data warehouse and data lakes

  • Experience creating reusable data pipelines for heterogenous data ingestions

  • Manage and maintain pipelines and troubleshoot data in data lake or warehouse

  • Provide visualization and analysis of data stored in data lake

  • Define and track KPIs and provide continuous improvement

  • Develop and maintain, tools, libraries, and reusable templates of data pipelines and standards for study level consumption by data configuration specialist

  • Collaborate with various vendors and cross functional teams to build and align on data transfer specification and ensure a streamlined process of data integration

  • Provide ad-hoc analysis and visualization as needed

  • 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.

  • Collaborate with system architecture team in designing and developing data pipelines as per business needs

  • Network with key business stakeholders on refining and enhancing the integration of structured and non-structured data

  • Provide expertise for structured and non-structured data ingestion

  • Develop organizational knowledge of key data sources, systems and be a valuable resource to people in the company on how to best integrate data to pursue company objectives.

  • Provides technical leadership on various aspects of clinical data flow including assisting with the definition, build, and validation of application program interfaces (APIs), data streams, data staging to various systems for data extraction and integration

  • Experience in creating data integrity and data quality checks for data ingestion

  • Coordinates with data base builders, clinical data configuration specialists and data management (DM) programmers ensuring accuracy of data integration per SOPs

  • Provide technical support / consultancy and end-user support, work with Information Technology (IT) in troubleshooting, reporting, and resolving system issues

  • Develop and deliver training programs to internal and external team, ensure timely communication of new and/or revised data transfer specs

  • Continuous Improvement/Continuous Development

  • Efficiently prepare and process large datasets for various end users for downstream consumption

  • Understand end to end requirements for stakeholders and contribute to process and conventions for clinical data ingestion and data transfer agreements

  • 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

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

  • Assess and enable clinical data visualization software in the data flows

  • Performs other duties as assigned within timelines

  • Performs clinical data engineering tasks according to applicable SOPs (standard operating procedures) and processes.

Educational Qualification:

  • Bachelor's degree 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:

  • BS with 8+ years’ experience. Minimum of 5 years’ experience in data engineering, building data pipelines to manage heterogenous data ingestions or similar in data integration across multiple sources including collected data.

  • Experience with Python/R, SQL, NoSQL

  • Cloud experience (i.e. AWS, AZURE or GCP)

  • Experience with GitLab, GitHub

  • Experience with Jenkins, GitLab

  • Experience deploying data pipelines in the cloud

  • Experience with Apache Spark (databricks)

  • Experience setting up and working with data warehouse, data lakes (eg: snowflake, Amazon RedShift etc.,)

  • Experience setting up ELT and ETL

  • Experience with unstructured data processing and transformation

  • Experience developing and maintaining data pipelines for large amounts of data efficiently

  • Must understand database concepts. Knowledge of XML, JSON, APIs.

  • Demonstrated ability to lead projects and work groups. Strong project management skills. 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

  • Strong Project Management skills

  • Strong understating of end-to-end processes for data collection, extraction and analysis needs by end users

  • Strong ability to communicate with cross functional stakeholders

  • Strong ability to develop technical specifications based on communication from stakeholders

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

  • Good knowledge of office software (Microsoft Office).

  • Experience creating custom functions Python/R

  • Cloud computing (AWS, Snowflakes, Databricks)

  • Ability to visualize large datasets

  • R shiny/Python App experience a plus

Preferable but not required:

  • Experience developing R shiny and Python apps

  • Experience with Hadoop

  • Experience with Agile development methods

Behavioral Competencies:

  • Is comfortable with ambiguity.

  • Excellent teamwork, organizational, interpersonal, conflict resolution and problem-solving skills.

Job Complexity:

  • Medium-High complexity project.

  • Occasional domestic/international travel to other Takeda sites, strategic partners, and therapeutic area events may be required.

Supervision:

  • Supervision required, should be able to function collaboratively (with guidance) with all levels of employees.

License/Certifications:

  • Preferred to have SAS or R or Python certification

Physical Demands:

  • Ability to sit and stand for long periods of time.

  • Carrying, handling, and reaching for objects.

  • Manual dexterity to operate office equipment i.e. computers, phones, etc.

Travel Requirements:

  • Requires approximately 1-2 domestic trips annually and up to 1 international trip.

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

Discover more attakedajobs.com

No Phone Calls or Recruiters Please.

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

Base Salary Range: $102,200.00 to $146,000.00, 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.

The final salary offered for this position may take into account a number of factors including, but not limited to, location, skills, education, and experience.

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

Boston, MA

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Company

Takeda is a global, values-based, R&D-driven biopharmaceutical leader headquartered in Japan, committed to discover and deliver life-transforming treatments, guided by our commitment to patients, our people and the planet. Takeda focuses its R&D efforts on four therapeutic areas: Oncology, Rare Genetics and Hematology, Neuroscience, and Gastroenterology (GI). We also make targeted R&D investments in Plasma-Derived Therapies and Vaccines. We are focusing on developing highly innovative medicines that contribute to making a difference in people’s lives by advancing the frontier of new treatment options and leveraging our enhanced collaborative R&D engine and capabilities to create a robust, modality-diverse pipeline. Our employees are committed to improving quality of life for patients and to working with our partners in health care in approximately 80 countries and regions.

For more information, visit https://www.takeda.com.

Stock Symbol: TAK

Company info
Website
Location
650 East Kendall Street
Cambridge
MA
02421
United States

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