- Takeda Pharmaceuticals (Boston, MA)
- …+ Significant experience in global drug development regulations, regulatory submissions, lifecycle management, compliance, business systems technology and ... bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Regulatory Project Management and Strategic Planning -… more
- AbbVie (Boston, MA)
- …demonstrates the ability to combine knowledge of scientific, regulatory & business issues to enable development and commercialization of products that are ... are effectively implemented and maintained in line with changing regulatory and business needs. Responsibilities: + This...and supports the Global Regulatory Lead (GRL, Director ), in the development & execution of… more
- Medtronic (Boston, MA)
- …you need to own your future success. Together, we can transform healthcare. The Senior Director of Regulatory Affairs will lead the Regulatory team for ... to market. It involves creating, managing and executing global regulatory strategies for new product development as...responsible for leading, developing and mentoring a team of regulatory professionals. The Robotic Surgical Business Unit… more
- AbbVie (Boston, MA)
- …@abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Director , Global Regulatory Lead, is responsible for developing and ... with global regulatory requirements. Manages compounds through all phases of development , including post approval and throughout the life cycle of the product.… more
- Sanofi Group (Cambridge, MA)
- …and external stakeholders to identify areas important to Sanofi and pharmaceutical business , development of policy positions, creation and execution of advocacy ... impact on the environment advise internal stakeholders on evolving regulatory policy issues, and more! The Director ...Provide support and leadership on additional projects concerning the development , status and impact of regulatory policy… more
- Sanofi Group (Cambridge, MA)
- About the Role The Associate Director , US Regulatory Affairs (RA) serves as the regulatory lead on relative Review Committees (RCs), for products in the Rare ... promotion of prescription drugs and biologics. Essential Functions + Represents Global Regulatory Affairs (US RA AdPromo) as a member of cross-functional brand and… more
- Sanofi Group (Cambridge, MA)
- The Associate Director RA serves as the regulatory lead on Review Committees (RCs). As the RC RA representative, work with brands on competitively positioning ... + Develops solutions to complex promotional issues by utilizing scientific and regulatory knowledge to support business objectives and initiatives while… more
- Sanofi Group (Cambridge, MA)
- **About the job** **Our team** The team is involved in developing and executing regulatory strategies for Tzield in life cycle development stages and post ... objectives. + Enables the GRL by providing quality regulatory input and position to internal business ... partners, including but not limited to the clinical development teams, commercial and Global Regulatory Team… more
- Sanofi Group (Cambridge, MA)
- …delivery of business objectives. + Enables the GRL by providing quality regulatory input and position to internal business partners, including but not ... limited to the clinical development teams, commercial and Global Regulatory Team...projects + Liaises with clinical, commercial, and other internal business partners in partnership with the GRL to enable… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …arrangements with external service providers and partner companies. **Due Diligence, Business Development & Alliance Projects** + Participate, conduct and ... best of my knowledge. **Job Description** **Job Description for Senior Medical Director , Clinical Science, Marketed Products Development ** As the Senior Medical… more
- HUB International (Boston, MA)
- **Position Summary:** As a FinPath Director of Business Development , you will play a pivotal role in driving the adoption and distribution of the FinPath ... + Stay abreast of industry trends, competitor offerings, and regulatory changes affecting the retirement planning landscape, and leverage...and are challenged by the opportunity to grow the business + are focused on learning and development… more
- Merck (Boston, MA)
- …The Director will manage the entire cycle of clinical development , including: study design, placement, monitoring, analysis, regulatory reporting, and ... regulatory affairs, statistics, and manufacturing to manage clinical development projects; and + Assist the Senior Director...external researchers around the world + Travel on company business about twenty (20) percent of the time to… more
- Bristol Myers Squibb (Cambridge, MA)
- …centers, co-operative groups, vendors and government agencies + Represents department in business development due diligence and partner alliance management as ... development + Serving as principal functional author for Regulatory submissions, study reports, and publications + Independently synthesizes and/or contributes… more
- Bristol Myers Squibb (Cambridge, MA)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . ** Director , Development DMPK** Challenging. Meaningful. Life-changing. Those aren't ... across the globe. PCO is looking for a Scientific Director to join the Development DMPK group...project teams, including developing ADME strategies and implementing drug development plans. + Understanding of regulatory requirements… more
- Unilever (Boston, MA)
- Director of Package Development & Engineering Boston, MA (http://maps.google.com/maps?q=One+Design+Center+Place+Boston+MA+USA+02210) Description Diversity is a ... Opportunity/Employer/Veterans/Disabled. The role is responsible for leading the Package Development & Engineering team and overseeing the planning, execution, and… more
- Bristol Myers Squibb (Cambridge, MA)
- …centers, co-operative groups, vendors and government agencies + Represents department in business development due diligence and partner alliance management with ... support development + Serving as principal functional author for Regulatory submission, study reports, and publications + Provides oversight and medical… more
- Merck (Boston, MA)
- …project work, the Associate Director is expected to contribute to ongoing business process improvement and talent development in Global Project and Alliance ... **Job Description** The drug development Project Manager is part of Global Project...organization of our company. **Position Description/Summary:** The GPAM Associate Director , Project Manager, is a core member of Early… more
- Prime Therapeutics (Boston, MA)
- …passion and drives every decision we make. **Job Posting Title** Senior Director , Product Development & Innovation **Job Description Summary** Provide leadership ... ongoing product maintenance. Through the use of full life-cycle product development , creates tangible business strategies, facilitates planning activities,… more
- Point32Health (Canton, MA)
- …+ Primary accountability for ensuring compliance to all relevant requirements **Staff Development ** + The Director must develop and maintain a highly ... the administrative budget for the Appeals and Grievances Department + Participate in the development of the annual business plan with a continuous focus on… more
- J&J Family of Companies (Boston, MA)
- Director , Early Development Leader - Hematology, Oncology Data Sciences & Digital Health - 2406180587W **Description** Johnson & Johnson's Innovative Medicine is ... recruiting for a Director of Oncology Data Science. You will report to...area partners (eg, Translational research, Precision Medicine and diagnostics, Regulatory Affairs, Market Access, Clinical Development ) to… more