- Merck & Co. (Montgomery County, PA)
- …described in the Pipeline Advertisemen We are currently recruiting for several Associate Director positions within US Marketing, covering Physician (HCP), ... collaborating across multiple stakeholders (including sales, marketing operations, Legal, Regulatory , Medicals, etc.) to drive promotional execution. This AD will… more
- Merck & Co. (Philadelphia, PA)
- Job DescriptionUnder the guidance of an Executive Director , within the Value & Implementation (V&I) Outcomes Research team the incumbent has the following ... of patient reported outcomes, epidemiological studies and economic modeling.The Associate Principal Scientist also works closely with Product Development Teams,… more
- CSL Behring (King Of Prussia, PA)
- …committed to developing therapies that make a meaningful difference worldwide. The Associate Director Clinical Operations Lead is accountable for the development ... and may take on additional responsibilities as defined by the Senior Director Clinops Program Lead. **Main Responsibilities:** + Clinical Operations Strategy: Design… more
- Merck & Co. (North Wales, PA)
- … Vice President, Clinical and Development Digital Solutions (CDDS IT), the Executive Director , Digital Regulatory and Safety, will lead our efforts in ... transforming regulatory submissions and pharmacovigilance through modern platforms and responsible...Develop and promote a multiyear product strategy for Digital Regulatory & Safety, aligning with IT and Research and… more
- CSL Behring (King Of Prussia, PA)
- The Associate Director , Vendor Governance is responsible for establishing and leading a new CoE focused on external service provider/vendor operational ... enable transparency, accountability, and alignment with enterprise strategy and regulatory expectations. **Main Responsibilities & Accountabilities:** Governance Framework Development… more
- CSL Behring (King Of Prussia, PA)
- …collection and submit all reports needed for compliance. 4. Work with Senior Director , Policy Advocacy & Government Affairs, & Legal to interpret and implement ... of biotech/pharmaceutical experience. **Experience** + Strong knowledge of the regulatory requirements for MDRP, Medicare/IRA, Veteran's Healthcare Act, and other… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe USDA Compliance Subject Matter Expert (SME) - Associate Director , will report to the Animal Health Global Quality Compliance and Technical ... GxP compliance concerns.Maintain up-to-date knowledge base with respect to emerging regulatory trends and changes in regulations and standards to incorporate into… more
- Merck & Co. (North Wales, PA)
- …Source Management Business Operations Lead is expected to understand the end-to-end regulatory submission process. The main focus will be on document production ... industry experience, at least 6 of those in a regulatory and/or compliance area and experience with technical systems...industry experience at least 6 of those in a regulatory and/or compliance area and experience with technical systems… more
- Merck & Co. (North Wales, PA)
- …of Channel Management, Distribution, Channel Solutions, Compliance & Customer Support. This director leads a team of Associate Directors and Sr. Specialists, ... & Sr. Specialists and guides and instructs the National Account Director /Executives, Customer Managers, Associate Directors, and Customer Account Representatives… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **Position Overview** The Associate Director is responsible for ensuring that Primary Market Research, Competitive Intelligence, and Data ... and procedures, and governing body rules and standards. The Associate Director will: + Be a champion...project workflows in core markets. + Support the Executive Director with internal audits, regulatory inspections and… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** We are looking for an experienced Associate Director , Program Manager to join our team. This successful candidate will ... in R&D functions (eg, Clinical Research, Early Development, Medical Affairs, Pharmacovigilance, Regulatory Affairs, etc.) + At least three years of experience in… more
- Organon & Co. (Plymouth Meeting, PA)
- …INDs, briefing books and other regulatory documents, as applicable. The Associate Director , Biopharmaceutics will be the primary author for module 2.7.1 ... **Job Description** **The Position** The Associate Director , Biopharmaceutics will provide expert...responsible for contributing to and reviewing clinical modules for regulatory submissions, contribute the authoring and review of Investigator… more
- Organon & Co. (Plymouth Meeting, PA)
- …development programs with early clinical development, late-clinical development, regulatory affairs, safety and pharmacovigilance, Chemistry, Manufacturing and ... be responsible for reviewing and authoring non-clinical and clinical modules for regulatory submissions, briefing books and other regulatory documents, as… more
- Organon & Co. (Plymouth Meeting, PA)
- …Reporting to the Director or Executive Director in Organon Regulatory Chemistry, Manufacturing and Controls (CMC), the Associate Principal Scientist is ... responsible for developing and implementing Regulatory Chemistry, Manufacturing & Controls (CMC) strategies for assigned small molecule or biological products in… more
- Merck & Co. (North Wales, PA)
- …and global core functions of GMI with guidance from senior GMI colleagues (eg, Associate Director , Director , and/or Director , Team Lead).Responsibilities ... has an advanced educational background and reports into the Director , Team Lead.- The responsibilities and activities of the...transparency in the EU and US (in partnership with Regulatory Affairs) and submissions to CMS for price negotiations… more
- Organon & Co. (Plymouth Meeting, PA)
- …**The Position?** Reporting to the Director in Organon Regulatory CMC,?the Associate Principal Scientist is responsible for?developing and?implementing ... in accordance with global regulations and?guidance, and?Organon procedures.? The Associate Principal Scientist will lead the?preparation and submission of CMC… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** The role of Associate Director , Dermatology Outcomes Research Epidemiology and Economics will report to the headquarters ... Director of Medical Affairs Outcomes Research. Focusing on Dermatology,...priorities. Developing and implementing patient-centred endpoints strategies, working with regulatory , Value Strategy Assessment (VSA's) and contracting. The role… more
- University of Pennsylvania (Philadelphia, PA)
- …wealth of health and wellness programs and resources, and much more. Posted Job Title Associate Director , Regulatory Job Profile Title Associate ... Job Description Summary With the oversight of the Director , the Associate Director for Regulatory Affairs will oversee the portfolio of clinical research… more
- J&J Family of Companies (Spring House, PA)
- …We are searching for the best talent for a **Senior Manager/ Associate Director ** , ** Regulatory Medical Writing** within ... Reporting (IDAR) business. This role will support our Immunology Regulatory Medical Writing area. **The position can be located...+ Writing or coordinating all types of clinical and regulatory documents, taking a proactive or lead role in… more
- J&J Family of Companies (Spring House, PA)
- …to developing innovative solutions and critical insights to support clinical programs and regulatory submissions. This Associate Director role, sitting on ... https://www.jnj.com/innovative-medicine Johnson & Johnson Innovative Medicine is recruiting for an ** Associate Director ,** **R&D Data Science & Digital Health -… more
