Talent.com
Associate Director - Analytics, Global Regulatory Affairs

Associate Director - Analytics, Global Regulatory Affairs

TakedaBoston, MA, United States
2 days ago
Job type
  • Full-time
Job description

Associate Director - Analytics, Global Regulatory Affairs

Overview

Base pay range : $137,000.00 / yr - $215,270.00 / yr. Location : Massachusetts - Virtual. This role involves strategic and operational oversight of custom analytics deliveries from Global Regulatory Affairs, including Business Intelligence solutions and related semantic layer dependencies.

Responsibilities

  • Responsible for strategic and operational oversight of the semantic layer and custom analytics capabilities in alignment with the Global Regulatory Analytics lead.
  • Work with primary business stakeholders to strategically align, shape and optimize requests for organizational and pre-existing solution alignment.
  • Support in-flight resources to understand and document data & insight requirements and technical specification needs.
  • Monitor, facilitate, and report on key initiatives / deliveries across multiple stakeholders following existing processes, best practices, and timelines.
  • Conduct group workshops, focused discussions, interviews and surveys for critical initiatives and roadmap development.
  • Build and establish key strategic relationships within the business and IT teams.
  • Establish best practices and industry / company standards for improving operational efficiency.

Core Profile

  • Ability to profile uses of operational process data and mash-up with behavioral data when required.
  • Visionary in determining how solution components fit together and driving integration across business processes.
  • Strong communication skills, customer-focused, metrics-driven, and able to discuss costs and trade-offs with customers and the GRA Analytics Team.
  • Ability to understand, plan, and collaborate on evolutionary paths for solution integrations, new technology insertions, and risk mitigation.
  • Essential Communicative Qualities

  • Well-respected and influential; able to communicate and influence peers, senior IT and business leaders.
  • Emphasis on methodology, modeling, and governance; knowledgeable in architectural and data modeling principles.
  • Technologically and politically neutral; capable of engaging with technical experts impartially.
  • Articulate, persuasive, and a good facilitator; able to educate and present ideas clearly.
  • Enthusiastic about technology, systems analysis and design; committed to the mission of the Global Regulatory Affairs Analytics team.
  • Business Qualifications

  • Strong business acumen with interpersonal, leadership, and teamwork skills.
  • Excellent oral and written communication and presentation skills.
  • Experience in Shared Services as a delivery model, with awareness of costs, chargeback models and quality considerations.
  • Proven experience leading high-profile, dynamic projects involving technology development.
  • Team player capable of influencing at all organizational levels to achieve consensus.
  • Self-starter who can work independently in a fast-paced environment and deliver actionable solutions.
  • Minimum Requirements / Qualifications

  • Minimum 8 years of experience in the pharmaceutical industry, including at least five years as a business systems analyst working with software, AI, data integration, data analytics, and reporting technologies (e.g., Informatica, MicroStrategy, IBM, SAS, Alteryx, Dataiku, Power BI, Tableau, Python).
  • Working knowledge of systems analysis and process modeling techniques / tools (e.g., SSADM, DFD, ERD, Data Schemas, Data Normalization & Data Dictionaries).
  • Experience leading high-profile projects involving technology development from start to finish.
  • Ability to translate concepts into scoping blueprints and to elicit requirements from business users and data owners.
  • Experience with data governance, data ownership, risk and compliance functions and techniques.
  • Strong communication skills and the ability to work across Shared Services models with awareness of costs and quality.
  • Self-starter with the ability to work independently in a fast-paced environment.
  • Education & Professional Credentials

  • BS in Business Administration – Management Information Systems
  • BS in Business Administration – General Administrative
  • BS / BA in Information Technology / Computer Science
  • Compensation & Benefits Summary

    We understand compensation is important. This summary reflects the U.S. base salary range and typical benefits. The actual base salary offered will depend on qualifications, experience, location, and other factors.

    Location

    Massachusetts - Virtual

    Job Details

  • Time Type : Full time
  • Worker Type : Employee
  • Job Exempt : Yes
  • EEO Statement

    Takeda is proud of 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 protected veteran status, in accordance with applicable laws.

    Locations : Massachusetts - Virtual

    #J-18808-Ljbffr

    Create a job alert for this search

    Associate Regulatory • Boston, MA, United States

    Related jobs
    • Promoted
    Associate Director, Regulatory Affairs Operations

    Associate Director, Regulatory Affairs Operations

    Kura OncologyBoston, MA, United States
    Full-time
    Are you ready to join a team committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines? At Kura Oncology, you have an opportunity to b...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director, Global Regulatory Affairs - GI & Inflammation

    Associate Director, Global Regulatory Affairs - GI & Inflammation

    Takeda Pharmaceutical Company LimitedBoston, MA, United States
    Full-time
    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 Tak...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director, Regulatory Affairs

    Associate Director, Regulatory Affairs

    Rhythm PharmaceuticalsBoston, MA, US
    Full-time
    Associate Director, Regulatory Affairs.Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocr...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director, Regulatory Compliance

    Associate Director, Regulatory Compliance

    Alnylam PharmaceuticalsCambridge, MA, United States
    Full-time
    The Associate Director, Regulatory Compliance will help develop and drive department-wide global regulatory compliance strategies, with input from key program, Regulatory, Quality and CMC stakehold...Show moreLast updated: 30+ days ago
    • Promoted
    Director, Global Regulatory Affairs, Neuroscience

    Director, Global Regulatory Affairs, Neuroscience

    Takeda PharmaceuticalBoston, MA, United States
    Full-time
    By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that.I provide in my application will be processed in line with.I further attest th...Show moreLast updated: 1 day ago
    • Promoted
    Associate Director, Global Regulatory Affairs, CMC Small Molecules

    Associate Director, Global Regulatory Affairs, CMC Small Molecules

    TakedaBoston, MA, United States
    Full-time
    Senior Manager, Global Regulatory Affairs, CMC Small Molecules.Join Takeda as a Senior Manager, Global Regulatory Affairs, CMC Small Molecules, where you will oversee the development and execution ...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director, Global Regulatory Affairs - GI & Inflammation

    Associate Director, Global Regulatory Affairs - GI & Inflammation

    Takeda PharmaceuticalsBoston, MA, US
    Full-time
    Defines, develops and leads global strategies to maximize global regulatory success towards achievement of program objectives for complex and / or multiple projects. Provides strategic and tactical ad...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director, Global Regulatory Affairs - GI & Inflammation

    Associate Director, Global Regulatory Affairs - GI & Inflammation

    TakedaBoston, MA, United States
    Full-time
    Defines, develops and leads global strategies to maximize global regulatory success towards achievement of program objectives for complex and / or multiple projects. Provides strategic and tactical ad...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director / Director, Regulatory CMC

    Associate Director / Director, Regulatory CMC

    CRISPR TherapeuticsBoston, MA, United States
    Full-time
    This position is a key leadership role for the development of the In Vivo franchise at CRISPR.Reporting to the Head of Regulatory Affairs CMC, you will work closely with cross-functional teams and ...Show moreLast updated: 17 days ago
    • Promoted
    Associate Director / Director - Upstream Process Development

    Associate Director / Director - Upstream Process Development

    EPM ScientificBoston, MA, US
    Full-time
    Associate Director / Director of Upstream Process Development.The Associate Director / Director of Upstream Process Development will lead the design, optimization, and scale-up of upstream processes fo...Show moreLast updated: 30+ days ago
    • Promoted
    • New!
    Associate Director, Global Regulatory Affairs - GI & Inflammation

    Associate Director, Global Regulatory Affairs - GI & Inflammation

    Takeda PharmaceuticalBOSTON, MA, United States
    Full-time
    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 Tak...Show moreLast updated: 16 hours ago
    • Promoted
    Senior Director Global Regulatory Affairs – Global Regulatory Lead – Neuroscience

    Senior Director Global Regulatory Affairs – Global Regulatory Lead – Neuroscience

    Takeda PharmaceuticalBoston, MA, United States
    Full-time
    By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that.I provide in my application will be processed in line with.I further attest th...Show moreLast updated: 1 day ago
    • Promoted
    Associate Director Global Regulatory Affairs

    Associate Director Global Regulatory Affairs

    LanceSoftCambridge, MA, US
    Full-time
    Associate Director Global Regulatory Affairs.Location : Cambridge, MA 02142 Duration : 06+ Months Hybrid or Remote possible (if hybrid, 2 days per week, 500 East Kendall, Cambridge, MA) 8 AM to 5 PM ...Show moreLast updated: 16 days ago
    • Promoted
    Associate Director, CMC Regulatory

    Associate Director, CMC Regulatory

    Mariana OncologyWatertown, MA, US
    Full-time
    We are seeking an experienced Associate Director, CMC Regulatory to join Marianas Chemistry, Manufacturing, & Controls organization, advancing personalized medicine and.This position provides l...Show moreLast updated: 2 days ago
    • Promoted
    • New!
    Associate Director, Global Regulatory Affairs

    Associate Director, Global Regulatory Affairs

    Takeda PharmaceuticalBOSTON, MA, United States
    Full-time
    By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that.I provide in my application will be processed in line with.I further attest th...Show moreLast updated: 4 hours ago
    • Promoted
    • New!
    Associate Director, Global Regulatory Affairs, Advertising and Promotion

    Associate Director, Global Regulatory Affairs, Advertising and Promotion

    Takeda PharmaceuticalBOSTON, MA, United States
    Full-time
    By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that.I provide in my application will be processed in line with.I further attest th...Show moreLast updated: 4 hours ago
    • Promoted
    Senior Manager / Associate Director, Regulatory Strategy

    Senior Manager / Associate Director, Regulatory Strategy

    EyePointWatertown, MA, US
    Full-time
    Be Seen And Heard At Eyepoint Pharmaceuticals.At EyePoint, leadership trusts our employees to get the job done.The patient-centric and award-winning approach we're taking in business fuels our succ...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director, Analytical Development

    Associate Director, Analytical Development

    VertexBoston, MA, US
    Full-time
    Associate Director, Analytical CMC Strategy.Vertex Pharmaceuticals is seeking a highly motivated, collaborative, and innovative Associate Director specializing in analytical CMC strategy to provide...Show moreLast updated: 30+ days ago