William Castroman
Dynamic and results-driven Technical Product Manager with 20 years of experience in developing and implementing R&D strategies for... | New York City Metropolitan Area, New York City Metropolitan Area, United States
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William Castroman’s Emails wc****@jn****.com
William Castroman’s Phone Numbers No phone number available.
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William Castroman’s Location New York City Metropolitan Area, New York City Metropolitan Area, United States
William Castroman’s Expertise Dynamic and results-driven Technical Product Manager with 20 years of experience in developing and implementing R&D strategies for information management product portfolios in Quality and Regulatory Affairs. Skilled in leading the integration of platforms such as Veeva RIM and Veeva QualityDocs. Proficient in leveraging AI and GenAI technologies to enhance regulatory submissions and interactions with global Health Authorities. Strong interpersonal and leadership skills with a proven track record of transforming business challenges into innovative solutions. Fluent in Spanish. Core Competencies: - Regulatory Strategy - Roadmap & Technology Prioritization - Product Portfolio Management - SDLC Methodologies (Agile) – GxP - Business Process Optimization - RFP / Vendor Selection Execution - Journey Maps & User Story Management - Vendor Management Technical Skills: - Veeva Submissions & Archive Integration - Veeva QualityDocs - Veeva QMS & Veeva eTMF - Regulatory Data Fabric - IA / Machine Learning Technology - Enterprise Dev & Test Management Tools - Regulatory Publishing Tools (Insight)
William Castroman’s Current Industry Johnson And Johnson
William
Castroman’s Prior Industry
Accenture
|
Centerline Partners
|
Knowledgent
|
Daiichi Sankyo
|
Virtua Pharma Technology
|
Johnson And Johnson
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Work Experience
Johnson And Johnson
Technical Product Manager - Regulatory Intelligence
Mon Feb 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Virtua Pharma Technology
Independent Consultant - Regulatory Affairs IT Lead
Sun Mar 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Feb 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)
Daiichi Sankyo
Quality Assurance Manager
Mon Jan 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Mar 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time)
Knowledgent
Business Process Engineering Consultant – R&D Informatics
Thu Oct 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Jan 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Centerline Partners
Management Consultant
Tue May 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Oct 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time)
Accenture
Consultant
Sun Aug 01 2004 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue May 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)Skills
Languages
William Castroman Email Addresses
FAQ About William Castroman
-
William Castroman is located at
New York City Metropolitan Area, New York City Metropolitan Area, United States -
William Castroman is a
Dynamic and results-driven Technical Product Manager with 20 years of experience in developing and implementing R&D strategies for information management product portfolios in Quality and Regulatory Affairs. Skilled in leading the integration of platforms such as Veeva RIM and Veeva QualityDocs. Proficient in leveraging AI and GenAI technologies to enhance regulatory submissions and interactions with global Health Authorities. Strong interpersonal and leadership skills with a proven track record of transforming business challenges into innovative solutions. Fluent in Spanish. Core Competencies: - Regulatory Strategy - Roadmap & Technology Prioritization - Product Portfolio Management - SDLC Methodologies (Agile) – GxP - Business Process Optimization - RFP / Vendor Selection Execution - Journey Maps & User Story Management - Vendor Management Technical Skills: - Veeva Submissions & Archive Integration - Veeva QualityDocs - Veeva QMS & Veeva eTMF - Regulatory Data Fabric - IA / Machine Learning Technology - Enterprise Dev & Test Management Tools - Regulatory Publishing Tools (Insight) Johnson And Johnson -
William Castroman currently works in the
Johnson And Johnson -
William Castroman specializes in
Dynamic and results-driven Technical Product Manager with 20 years of experience in developing and implementing R&D strategies for information management product portfolios in Quality and Regulatory Affairs. Skilled in leading the integration of platforms such as Veeva RIM and Veeva QualityDocs. Proficient in leveraging AI and GenAI technologies to enhance regulatory submissions and interactions with global Health Authorities. Strong interpersonal and leadership skills with a proven track record of transforming business challenges into innovative solutions. Fluent in Spanish. Core Competencies: - Regulatory Strategy - Roadmap & Technology Prioritization - Product Portfolio Management - SDLC Methodologies (Agile) – GxP - Business Process Optimization - RFP / Vendor Selection Execution - Journey Maps & User Story Management - Vendor Management Technical Skills: - Veeva Submissions & Archive Integration - Veeva QualityDocs - Veeva QMS & Veeva eTMF - Regulatory Data Fabric - IA / Machine Learning Technology - Enterprise Dev & Test Management Tools - Regulatory Publishing Tools (Insight) -
William Castroman speaks the following languages:
No languages available. -
William Castroman has prior experience in the following industries:
Virtua Pharma Technology , Daiichi Sankyo , Knowledgent , Centerline Partners , Accenture -
William Castroman has the following professional experience:
Johnson And Johnson , Virtua Pharma Technology , Daiichi Sankyo , Knowledgent , Centerline Partners , Accenture . -
You can view William Castroman’s
LinkedIn profile at LinkedIn URL. -
William Castroman’s work email addresses are
[email protected] . -
William Castroman works at
Johnson And Johnson
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