• AstraZeneca Pharmaceuticals (Gaithersburg, MD)
    …our people's exceptional skills with those of people from all over the globe. As an Associate Regulatory Project Director in Gaithersburg, MD , you'll ... capabilities to make a positive impact on changing patients' lives. Description: The Associate Regulatory Project Director (ARPD) is an experienced … more
    HireLifeScience (11/12/19)
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  • Takeda Pharmaceuticals International GmbH (Cambridge, MA)
    Associate Director , Project Management, Regulatory Affairs Vaccines Apply Now Job ID R0014086 Date posted 11/04/2019 Location Cambridge, Massachusetts By ... Privacy Policy and Terms of Use. Job Description OBJECTIVES: + Responsible for regulatory activities supporting the development of vaccine candidates in the US and… more
    Takeda Pharmaceuticals International GmbH (11/25/19)
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  • Takeda Pharmaceuticals International GmbH (Cambridge, MA)
    …Type Full time Job ID R0014086 PHYSICAL DEMANDS: ACCOUNTABILITIES: Associate Director , Project Management, Regulatory Affairs Vaccines By clicking the ... ?Apply? button, I understand that my employment application process with Takeda will commence and that I agree with Takeda?s more
    Takeda Pharmaceuticals International GmbH (11/25/19)
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  • Apex Systems (Lexington, MA)
    …therapeutics, is seeking an experienced and enthusiastic Director / Associate Director Regulatory Affairs Project Manager to join their growing ... Director / Associate Dir Regulatory Affairs... Director / Associate Dir Regulatory Affairs - Oncology...Regulatory , Medical Writing, CMC Regulatory , Ad-Promo Regulatory and RegOps) and with cross-functional project more
    Neuvoo (12/04/19)
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  • Gilead Sciences, Inc. (Seattle, WA)
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    Gilead Sciences, Inc. (11/25/19)
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  • Takeda (Cambridge, MA)
    OBJECTIVES: Responsible for regulatory activities supporting the development of vaccine candidates in the US and Canada, ex-US experience preferred but not ... essential. Manages regulatory projects and submissions for vaccine candidates Ensures that...and content for local label development. Responsible for assigned project /timeline planning and tracking of commitments. Responsible for communication… more
    Neuvoo (12/04/19)
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  • Ascendis Pharma A/S (Palo Alto, CA)
    …becoming a leading rare disease company. Ascendis Pharma is looking to hire an experienced Associate Director , Regulatory Affairs to join our team. This is ... exciting opportunity to join a rapidly growing, innovative company! Position Summary The Associate Director , Regulatory Affairs will be responsible for… more
    Neuvoo (12/04/19)
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  • Jazz Pharma (Palo Alto, CA)
    …resource for programming group to provide advice and support on regulatory submissions, complex programming tasks and standards. * Develop software validation ... Assist in development of standards for time and resource estimates for project planning. * Assist in development of training and onboarding statistical programmers.… more
    ZipRecruiter (11/16/19)
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  • Meet (San Francisco, CA)
    …bio-pharmaceutical focused on autoimmune/inflammatory disorders and oncology, seeking a motivated Associate Director / Director of Regulatory Affairs ... FDA and other regulatory authorities Build a Regulatory Affairs department, manage budgets and project ...a Regulatory Affairs department, manage budgets and project timelines, identify and address gaps in planning and… more
    Neuvoo (12/04/19)
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  • NYC Health + Hospitals (New York, NY)
    …experience. Description: Reporting to the Assistant Vice President for Accreditation and Regulatory Services, the Associate Director provides consultative ... and regulatory requirements and compliance issues. The Associate Director also collects, aggregates and analyzes...facility and central office staff on new and/or revised regulatory updates Accountable for project deliverables and… more
    Neuvoo (12/04/19)
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  • Jazz Pharma (Philadelphia, PA)
    …the area of product labeling for Jazz Pharmaceuticals. This position reports to the Associate Director , Regulatory Affairs Labeling and will be responsible ... and issue resolution * Under the direction of the Associate Director , Regulatory Affairs Labeling,... Affairs colleagues and Supply Chain colleagues * Provide project management to the Labeling Team throughout the entire… more
    ZipRecruiter (11/06/19)
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  • GForce Life Sciences (Medford, MA)
    Associate Director Project Manager, Research and Development, Oncology Summary Our client, a global leader in oncology, is looking for an experienced ... project manager to help lead several initiatives. The successful...within related functions (eg Clinical Science, Clinical Operations, Research, Regulatory , CMC, Marketing). 6-8+ years program management experience leading… more
    Neuvoo (11/30/19)
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  • Arrowhead Pharmaceuticals (Pasadena, CA)
    … agency interactions. The GRL will be responsible for providing day to day regulatory support to the project team and regulatory team management. ... The Position The Global Regulatory Lead (GRL) is responsible for facilitating global...skills and ability to deal with changing priorities Excellent project management skills Proficient in pertinent software & tools… more
    Neuvoo (12/04/19)
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  • GForce Life Sciences (Arlington, VA)
    Associate Director Project Manager, Research and Development, Oncology Summary Our client is looking for an experienced project manager to help lead a ... and interact across all levels of the organization and manage complex project timelines. Provides global program management and matrixed leadership to global,… more
    Neuvoo (12/03/19)
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  • GForce Life Sciences (Chicago, IL)
    Associate Director Project Manager, Research and Development, Oncology, Summary: Our client is looking for an experienced project manager to help lead a ... and interact across all levels of the organization and manage complex project timelines. Provides global program management and matrixed leadership to global,… more
    Neuvoo (12/03/19)
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  • AnaptysBio (San Diego, CA)
    regulatory filings in alignment with company timelines. Provide project management support and actively manage the relationships, performance and productivity ... this position is responsible for providing chemistry, manufacturing and control (CMC) project management for one or more of AnaptysBio's novel therapeutic antibody… more
    Neuvoo (11/30/19)
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  • Orchard Therapeutics (Menlo Park, CA)
    …date knowledge of regulatory CMC requirements and communicate changes in regulatory information to project teams and senior management Monitor, analyze, and ... Location: Menlo Park (US) Reporting to: VP Regulatory CMC Orchard Therapeutics Limited is a global...a cross-functional team environment with experience managing people and project teams; ability to work with remote teams Strong… more
    Neuvoo (12/02/19)
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  • Iris Diagnostics, Inc. (North Brunswick Township, NJ)
    …to develop project plans including resource identification, budget, facility and regulatory requirements to meet project goals and clinical timelines Lead ... diagnostic development partnerships with third parties from inception through regulatory approval in multiple jurisdictions Basic Qualifications Doctorate degree and… more
    Neuvoo (12/04/19)
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  • Kite Pharma (Emeryville, CA)
    Research Associate Director , Kite Research Operations ( Associate Director , Project Management) Kite, a Gilead Company, is a commercial-stage ... on behalf of the RT for the LE process. In addition, the Research Sr. Project Manager/ Associate Director may also contribute to Research Governance and… more
    Neuvoo (12/03/19)
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  • Daiichi Sankyo (Bernards, NJ)
    …veteran status, age, or any other characteristic protected by law. Job Title Associate Director Regulatory Affairs Strategy City Basking Ridge Functional ... issues. Prepare and review annual reports and supplements for marketed products. The Associate Director , Regulatory Affairs will liaise with the review… more
    Neuvoo (12/02/19)
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