Lead Report Developer Position Available In Suffolk, Massachusetts

Lead Report Developer
Employer
Takeda
Location
Boston, Massachusetts
Start date
May 19, 2025
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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’sPrivacy Noticeand 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 Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc.

for the following job opportunity:

JOB LOCATION

Cambridge, MA

POSITION

Lead Report Developer

POSITION DESCRIPTION

Takeda Development Center Americas, Inc. is seeking a Lead Report Developer with the following duties: Deliver pharmacovigilance (PV) reporting & analytic solutions for Takeda Patient Safety & Pharmacovigilance (PSPV); Identify and develop methods for statistics and AI/Machine Learning to support the department’s data needs; Solve business problems in drug safety which provide an increased understanding of such tools and techniques. Identify and document Global Pharmacovigilance reporting end-user system needs and requirements; Provide strategic technical input into development of roadmaps and plans for implementing Business Intelligence (BI) capabilities (reporting, interactive analysis views, dashboards, etc.) in response to global pharmacovigilance user requirements and/or regulatory guidance; Lead and perform user needs and requirements analysis, support construction and maintenance of BI solutions, using Oracle, Cognos, and other applicable technologies, which include definition of requirements, designs, source code development, unit testing, maintenance, and migration; Lead and execute tuning and optimization of Global reporting solutions, including identification for mitigating risks in proposed solutions; Lead and execute Global custom report and Global ad hoc query development; contribute to prioritization, planning, and execution of global reports; Lead complex Global system and data investigations, supporting end-user inquiry and Global Pharmacovigilance requirements; Provide strategic technical input into the definition and documentation of Global reporting development and related process standards, procedures, and best practices; Research and contribute to implementation of automated processes, driving for improved overall efficiency in all areas of Global PV Reporting and Analytics service delivery; Perform audit and inspection support related to Global PV Reporting and Analytics; Development, tracking, and reporting of quality metrics for Global PV reports; Provide strategic technical input and support of Global PV DB Reporting and Analytics technology projects as required; Provide mentoring, training and best practices for ad-hoc query and other Global report developers. Up to 100% remote work allowed.

REQUIREMENTS

Bachelor’s degree in Computer Science, Data Science, Pharmaceutical or Life Science or related field plus 5 years of related experience.

Prior experience must include:

Utilize knowledge of drug safety systems, including the underlying data model(s)to design, develop, document, test, and deploy custom reports, dashboards, and database views that meet user or regulatory requirements; Plan, manage, and implement small projects in accordance with software/system development life cycle principles; Contribute to computer systems validation activities as they relate to 21 CFR Part 11 & GxP compliance (e.g. user requirements gathering & definition, authoring of technical specification documents, authoring user acceptance tests); Analyze user feedback to identify and remediate issues with the configuration of the global safety database and its associated data. Full time. $145,000.00 – $228,000.00 per year. Competitive compensation and benefits. Qualified applicants can apply at jobs.takeda. Please reference job #

R0148087. EOE

Any individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210. LocationsBoston, MA Worker TypeEmployee Worker Sub-TypeRegular Time TypeFull time
Company For over 240 years, Takeda’s propensity to evolve has driven the next generation of innovation. Today, our organization spans the globe—colleagues across business units and functions face challenges head-on to deliver life-transforming treatments, guided by our commitment to patients, our people and the planet. As a values-based, R D-driven biopharmaceutical leader headquartered in Japan, we focus our 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. In addition to our R D efforts, we’re laser-focused on harnessing the power of data, digital, and technology to improve health outcomes for patients across the globe. Since our founding in Japan, integrity and putting patients first have been at the heart of our identity. We’re proud of our employees and their commitment to improving the quality of life for patients, and to working with our partners in health care in approximately 80 countries and regions. With each new breakthrough comes opportunities to develop your career, hone new skills, and create a brighter future For more information, visit jobs.takeda/ Company info