Lead Report Developer Position Available In Suffolk, Massachusetts

Job Description:

By clicking the “Apply” button, I understand that my employmentapplication process with Takeda will commence and that theinformation I provide in my application will be processed in linewith Takeda’s Privacy Notice and Terms of Use . I further attestthat all information I submit in my employment application is trueto the best of my knowledge. Job Description Pursuant to Section 20C.F.R. 656.10, you are hereby notified that an application forAlien Employment Certification will be filed by Takeda DevelopmentCenter Americas, Inc.

for the following job opportunity:

JOBLOCATION

Cambridge, MA

POSITION

: Lead Report Developer

POSITIONDESCRIPTION

: Takeda Development Center Americas, Inc. is seeking aLead Report Developer with the following duties: Deliverpharmacovigilance (PV) reporting & analytic solutions for TakedaPatient Safety & Pharmacovigilance (PSPV); Identify and developmethods for statistics and AI/Machine Learning to support thedepartment’s data needs; Solve business problems in drug safetywhich provide an increased understanding of such tools andtechniques. Identify and document Global Pharmacovigilancereporting end-user system needs and requirements; Provide strategictechnical input into development of roadmaps and plans forimplementing Business Intelligence (BI) capabilities (reporting,interactive analysis views, dashboards, etc.) in response to globalpharmacovigilance user requirements and/or regulatory guidance;Lead and perform user needs and requirements analysis, supportconstruction and maintenance of BI solutions, using Oracle, Cognos,and other applicable technologies, which include definition ofrequirements, designs, source code development, unit testing,maintenance, and migration; Lead and execute tuning andoptimization of Global reporting solutions, includingidentification for mitigating risks in proposed solutions; Lead andexecute Global custom report and Global ad hoc query development;contribute to prioritization, planning, and execution of globalreports; Lead complex Global system and data investigations,supporting end-user inquiry and Global Pharmacovigilancerequirements; Provide strategic technical input into the definitionand documentation of Global reporting development and relatedprocess standards, procedures, and best practices; Research andcontribute to implementation of automated processes, driving forimproved overall efficiency in all areas of Global PV Reporting andAnalytics service delivery; Perform audit and inspection supportrelated 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 DBReporting and Analytics technology projects as required; Providementoring, training and best practices for ad-hoc query and otherGlobal 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 ofrelated experience.

Prior experience must include:

Utilizeknowledge of drug safety systems, including the underlying datamodel(s)to design, develop, document, test, and deploy customreports, dashboards, and database views that meet user orregulatory requirements; Plan, manage, and implement small projectsin accordance with software/system development life cycleprinciples; Contribute to computer systems validation activities asthey relate to 21 CFR Part 11 & GxP compliance (e.g. userrequirements gathering & definition, authoring of technicalspecification documents, authoring user acceptance tests); Analyzeuser feedback to identify and remediate issues with theconfiguration of the global safety database and its associateddata. Full time. $145,000.00 – $228,000.00 per year. Competitivecompensation and benefits.

Qualified applicants can apply athttps:

//jobs.takeda.com . Please reference job

R0148087. EOE

Anyindividual may provide documentary evidence bearing on thisapplication, with information on available workers and informationon wages and working conditions, to the Certifying Officer, U.S.Department of Labor, Employment and Training Administration, Officeof Foreign Labor Certification, 200 Constitution Avenue, NW, RoomN-5311, Washington, DC 20210. Locations Boston, MA Worker TypeEmployee Worker Sub-Type Regular Time Type Full time