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Senior Director, Global Regulatory Portfolio Lead, Global Regulatory Affairs

Company: Takeda Pharmaceutical
Location: Lowell
Posted on: November 12, 2021

Job Description:

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 and . I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionAre you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda.- Join us as a Senior Director, Global Regulatory Portfolio Lead, Global Regulatory Affairs - Rare Genetics and Hematology. This is a remote positio-Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As a Senior Director working on the Global Regulatory Affairs Rare Genetics and Hematology team, you will be empowered to provide leadership and development to global regulatory leads to ensure innovative and robust global regulatory strategies are developed to maximize regulatory success and minimize time to approval, and a typical day will include:-OBJECTIVES/PURPOSE - Provides leadership and development to global regulatory leads to ensure innovative and robust global regulatory strategies are developed to maximize regulatory success and minimize time to approval.- Develops best practices and creates a strong regulatory community across the broader Global Regulatory Affairs (GRA) organization.- Serves as an influential leader within Takeda and external to Takeda, contributing to cross-functional initiatives and influencing the field as applicable.ACCOUNTABILITIES

  • The Sr. Director will be responsible for managing direct reports and overseeing all global and US submission for an assigned portfolio of projects . These include ensuring that the direct reports have defined, developed and clearly communicated appropriate global strategies to maximize global regulatory success. The role may serve as an interim GRL on a global project team on a as needed basis.
  • Partner with direct reports to ensure global market access consideration are being addressed- and provide senior strategic input to interactions with joint regulatory/health agency/HTA bodies on product specific value evidence topics, as applicable.
  • Ensures line management and key stakeholders are apprised of developments that may impact regulatory success, exercising sound judgement and communicating in a professional and timely manner. Demonstrates ability to anticipate risks and responsible for developing solutions to identified risks and discussing with direct reports and management; understands probabilities of technical success for the solutions.
  • Effectively represent the Global Regulatory Affairs (GRA) function in senior level interactions at internally governance technical review committees, key global health authority meetings and external partners.
  • Accountable for working with regulatory regional leads, other functions and vendors to ensure global regulatory submissions are provided to local Takeda affiliates in compliance with local regulations and to maintain compliance for products.
  • Participates with influence in or leads departmental and cross-functional task-forces and initiatives.- Influence non-direct reports within Therapeutic Area, across GRA and across R&D.
  • Provide regulatory strategy support to diligence for licensing opportunities as appropriate
  • Monitor and anticipate trends that impact both the regulatory and access environments to strengthen product development plan(s) and adopt regulatory strategies in a timely manner.
  • Responsible for demonstrating Takeda leadership behaviors.DIMENSIONS AND ASPECTS Technical/Functional (Line) Expertise
    • Comprehensive understanding of the pharmaceutical industry and global regulatory strategy experience.Leadership
      • Demonstrated ability to work across functions, regions and cultures
      • Functional level leadership with the ability to inspire, motivate and drive results
      • Excellent communicator, able to persuasively convey both ideas and data, verbally and in writing
      • Proven skills as an effective team player who can engender credibility and confidence within and outside the company
      • Ability to distil complex issues and ideas down to simple comprehensible terms
      • Demonstrates leadership presence and confidence
      • Embraces and demonstrates a diversity and inclusion mindset and role models these behaviors for the organization
      • Builds teams across functions and geographies with individuals who have the right skills and experience to deliver on key organizational initiatives.
      • Invests time in helping others to enhance their skills and perform at a higher levelDecision-making and Autonomy
        • Decision making responsibilities:
        • Provide input to highly complex decisions that impact the functional area
        • Accountable for decision making for designated function
        • Ability to seek diverse input from multiple constituents and stakeholders to drive innovative solutions
        • Ability to incorporate feedback and ensure decisions are implemented swiftly to yield flawless execution-
        • Accountable for providing input to and implementing vision and strategy for designated scope-making, complexity of decisions, impact of decisions, problem-soliving)Interaction
          • Effectively navigates the changing external and internal environment and leads others through change by creating and inspiring and engaging workplace
          • Cultivates a broad network of relationships throughout Takeda, with affiliates and external partners, in the industry and area of expertise.
          • Effectively represents function in negotiations with the ability to resolve conflict in a constructive manner
          • Ability to build strong relationships and collaborate effectively with other interfacing Takeda functionsInnovation
            • Forward thinking with the ability to recommend, influence and implement organizational change and continuous innovation
            • Comfortable challenging the status quo and bringing forward innovative solutions
            • Ability to take risks implementing innovative solutions, accelerating time to market
            • Identifies opportunities and anticipates changes in the business landscape through an understanding and ongoing assessment of the environment affecting the business.
            • Role models respect and inclusion, creating a culture that fosters innovationComplexity
              • Ability to work in a global ecosystem (internal and external) with a high degree of complexity
              • Deep expertise required
              • Ability to see and understand broader, enterprise level perspective-EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:-
                • Advanced degree in a scientific subject area (e.g. MSc, PhD, PharmD, MD) with global oncology regulatory experience preferred.- BA accepted.
                • 12+ years of pharmaceutical industry experience.- This is inclusive of 10 years of regulatory experience or combination of 8+ years regulatory and/or related experience.-
                • Preferred experience in reviewing, authoring, or managing components of regulatory submissions.-
                • Solid working knowledge of drug development process and regulatory requirements.- Knowledge of FDA, EU, Canada, ROW and post-marketing a plus.-
                • Understand and interpret complex scientific issues across multiple projects as it related to regulatory requirements and strategy.
                • Understands and interprets scientific data as it relates to regulatory requirements and strategy for assigned projects and provides knowledge and expertise to guide team in established and building appropriate global regulatory strategy.
                • Strong oral and written communications, managing and adhering to timelines, negotiation skills, integrity and adaptability.
                • Demonstrates acceptable skills with increasing independence in the area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively identifies regulatory issues; offers innovative
                • -solutions and strategies, including risk mitigation strategies.
                • Must work well with others and within global teams.-
                • Able to bring working teams together for common objectives.
                • Acceptable and independent skills in the area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively identifies regulatory issues; offers creative solutions and strategies, including risk mitigation strategies.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 ProgramsLocation and Salary Information:
                    • Location(s): Remote
                    • Base Salary Range: $240K-$270K based on candidate professional experience level. Employee may also be eligible for Short Term and/or Long Term incentive benefits. Employees are eligible to participate in Medical, Dental. Vision, Life Insurance, 401(k), Charitable Contribution Match, Company Holidays, Personal & Vacation Days, Student Loan Repayment Program and Paid Volunteer Time Off
                    • If candidate is not eligible for any benefits or other comp., those can be excluded -This posting is made in compliance with Colorado's Equal Pay for Equal Work Act, C.R.S. - 8-5-101 et seq.-Empowering Our People to ShineLearn more at .No Phone Calls or Recruiters Please.#LI-LC1Effective November 1, 2021, absent an approved religious or medical reason, all US office-based and lab-based Takeda employees who work fully on-site or in a hybrid model (as determined by Takeda) must be fully vaccinated to work at a Takeda site or to engage with Takeda colleagues or anyone else on behalf of Takeda. As of the same date, absent an approved religious or medical reason, US field-based employees, employees must be fully vaccinated in order to continue in their current roles.- US employees who work at a Takeda manufacturing facility, and those who work at a BioLife center or BioLife lab, may be subject to different guidelines. Candidates are encouraged to speak with their recruiter to seek further information on the applicable guidelines for the Business Unit/Function for which they have applied.EEO StatementTakeda 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.LocationsBoston, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time

Keywords: Takeda Pharmaceutical, Lowell , Senior Director, Global Regulatory Portfolio Lead, Global Regulatory Affairs , Executive , Lowell, Massachusetts

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