- Merck & Co. (Lower Gwynedd, PA)
- …Us: The Discovery, Preclinical and Translational Medicine Operations (DPTM) is seeking an Associate Director to lead the Molecular lab within the Late ... utilized to generate pivotal safety and efficacy clinical patient data required for regulatory filings. As the AdVAnce facility will not be fully constructed and… more
- Merck & Co. (Millsboro, DE)
- … regulatory inspections (USDA, DEA, DNREC, etc.) of animal facilities and program reviews is required.PurposeThis Associate Director will report to ... Job DescriptionOur company seeks to add an Associate Director . Veterinarian Services at our...well as for the veterinary care and animal husbandry program at our company's Millsboro Animal Health facilities. This… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …development. Are you ready to maximize your potential with us? The Position The Associate Director , Data & Analytics Governance is responsible for the governance ... skills to ensure vision is maintained across various NNI functions. Relationships The Associate Director , Data & Analytics Governance reports to the Senior … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …personal development. Are you ready to maximize your potential with us? The Position The Associate Director will be the lead who is responsible for ensuring that ... Reports to the Sr. Director , Patient Support Solution Quality/Safety Associate Director . Interacts with colleagues within Patient Support Programs, Patient… more
- Merck & Co. (Rahway, NJ)
- …with key partner organizations (as a lead Global Clinical Supply Planning program representative) such as clinical development, regulatory , quality and other ... clinical development teams and the operational/executional arms within the business. The Program Clinical Supplies Project Manager serves as the primary program… more
- Genmab (NJ)
- …the development of the clinical development plan (CDP) Author components with Medical Director and reviewer of clinical and regulatory documents and registration ... aspects of clinical development) working closely with the Medical Director and other cross-functions to provide high-quality and timely deliverablesResponsibilities… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …plays a critical role in supporting the Ethics & Compliance (E&C) program by strategically identifying, assessing, and mitigating the organization's top risk areas. ... in developing partnerships and strategies to promote the NNI Ethics & Compliance program and the Novo Nordisk Way, fostering a culture committed to ethics and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans, ... Initiates contact w/KOL and prepares material for KOL interactions on a program based need; Involvement with in-licensing and acquisitions on individual due… more
- Merck & Co. (Rahway, NJ)
- …portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team ... formulation, manufacturing process, and primary packaging to enable phase appropriate regulatory filings for large molecule sterile products. -These sterile products… more
- Merck & Co. (Rahway, NJ)
- …oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team ... portfolio and influence bridging strategies across the portfolio. The Biopharmaceutics Director will work with their direct reports to proactively develop and… more
- Merck & Co. (Rahway, NJ)
- …sites, manufacturing investigations, process validation, and authoring of regulatory submissions. -Under the general scientific and administrative direction ... of Director in the CCFS group and working in conjunction...individual will support late stage and commercial large molecule program activities within CCFS. The individual will be responsible… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …integrity, and timelines for assigned studies and escalates issues to the Associate Director of Medical Coding to gain resolution. Functional Expertise:Study ... conventions. Reviews and submits DS Medical Coding synonym list update requests to the Associate Director of Medical Coding to ensure accuracy and consistency of… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director of Biologics Potency in Analytical Research & Development is responsible for providing strategic and technical leadership for a portion ... partnering to build a culture of innovation and inclusion.-The Director reports to the Executive Director , Cell...responsible for a team of approximately 10-15 senior and associate level scientists in Rahway, New Jersey. -The position… more
- Takeda Pharmaceuticals (Boston, MA)
- …is possible in order to bring life-changing therapies to patients worldwide. As an Associate Director , Global Regulatory Affairs Marketed Products you will ... define, develop and lead global strategies to maximize global regulatory success towards achievement of program objectives...field as applicable. **How you will contribute:** + The Associate Director will be responsible for increasingly… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Regulatory Lead, GI & Inflammation where you ... define, develop, and lead global strategies to maximize global regulatory success towards achievement of program objectives...field as applicable. **How you will contribute:** + The Associate Director will be responsible for complex… more
- Guidehouse (Mclean, VA)
- …to 25% **Clearance Required** **:** None **What You Will Do** **:** ** Associate Director - Regulatory Rate Design.** Responsibility for delivering ... to bring comprehensive enhancements to our clients. In this ** Associate Director - Regulatory Rate Design** role,...+ Experience as expert witness on utility rate and program design \#LI-RE1 The annual salary range for this… more
- Abbott (Alameda, CA)
- …work for diversity, working mothers, female executives, and scientists. **The Opportunity** This ** Associate Director Regulatory Affairs - APAC** will work ... Alameda, CA, location in the Diabetes Division. As a manager, the function of an Associate Director Regulatory Affairs, APAC (Asia Pacific) is to combine… more
- Takeda Pharmaceuticals (Lexington, MA)
- …to the best of my knowledge. **Job Description** ** Associate Director , US Advertising & Promotion Regulatory Review** **Takeda Pharmaceutical** **Lexington, ... MA or Exton, PA** **About the role:** Join Takeda as an Associate Director , US Advertising & Promotion Regulatory Review out of our Lexington, MA or Exton,… more
- Takeda Pharmaceuticals (Columbus, OH)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning - GI2 ... Project Management leadership, oversight, direction and planning. + Directly supports program GRL by ensuring project management and regulatory operational… more
- Abbott (Alameda, CA)
- …work for diversity, working mothers, female executives, and scientists. **The Opportunity** This ** Associate Director Regulatory Affairs - US New Product ... (https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html) student debt program and FreeU… more
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