- Merck & Co. (Upper Gwynedd, PA)
- …Office (PMO); and Administrative Professionals. Position Description/Summary: The GPAM Associate Director, Value & Implementation Project Manager (VIPM), is a ... to progress the R&D pipeline and realize its full potential. The Associate Director is expected to provide project management leadership and drive cross-functional… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …Learn more about Life at Olympus: https://www.olympusamerica.com/careers . **Job Description** The Sr . Clinical Trial Coordinator ( Sr . CTC) will be responsible ... of a clinical study by carrying out day-to-day study activities. The Sr . CTCwill develop, implement, and coordinate study procedures to successfully manage clinical… more
- CSL Behring (King Of Prussia, PA)
- …the guidance of the Publications Director, you will partner with Medical Affairs leaders, Compliance, Clinical, HEOR, and other functions to build efficient ... SOPs, and governance frameworks that ensure scientific integrity and regulatory compliance. You will also drive innovation in publication...and enhance our scientific impact globally. As a more senior member of the publications team, you will also… more
- Merck & Co. (Upper Gwynedd, PA)
- …studies.Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... development projectsAssist the Senior Director, Associate Vice-President/Vice-President and Product Development Team Lead in ensuring that appropriate corporate… more
- CSL Behring (King Of Prussia, PA)
- The Associate Director, Commercial Data Science & AI is crucial in driving the overall strategy for (Gen)AI tools and technologies within CSL. This individual will ... this role you will be reporting in to the Senior Director of Commercial Business Analytics Reporting & Data...use cases) In close partnership with ABCIA Commercial, Medical Affairs , and Market Access teams to ensure solutions are… more
- CSL Behring (King Of Prussia, PA)
- …required data collection and submit all reports needed for compliance. 4. Work with Senior Director, Policy Advocacy & Government Affairs , & Legal to interpret ... of biotech/pharmaceutical experience. **Experience** + Strong knowledge of the regulatory requirements for MDRP, Medicare/IRA, Veteran's Healthcare Act, and other… more
- Teleflex (Wyomissing, PA)
- Sr . Regulatory Affairs Associate **Date:** Nov 24, 2025 **Location:** Wyomissing, PA, US **Company:** Teleflex **Expected Travel** : None **Requisition ... in patients' lives. **Position Summary** The Sr Regulatory Affairs (RA) Associate will...quality system compliance requirements. The Senior RA Associate will partner with Product Management Regulatory … more
- Sumitomo Pharma (Harrisburg, PA)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director, Regulatory Affairs (Oncology).** The Associate ... Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/She will...Comfortable presenting to all levels of the organization including Senior Management. **Education and Experience** + Bachelor's degree in… more
- University of Pennsylvania (Philadelphia, PA)
- … Regulatory Job Description Summary With the oversight of the Director, the Associate Director for Regulatory Affairs will oversee the portfolio of ... clinical research undertaken within the department/division. The Associate Director for Regulatory Affairs assists the Director in providing direction and… more
- Penn Medicine (Philadelphia, PA)
- …and Delaware. Reporting to the Senior Director of Government Relations and Regulatory Affairs , the Associate Director helps develop and implement Penn ... the Senior Director of Government Relations and Regulatory Affairs on strategic initiatives and short-... strategy that aligns with organizational goals, including the Associate Vice President of Government and Community Relations and… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- …Integration and Portfolio Management** + Serve as a strategic advisor to senior leadership on medical affairs priorities, risks, and opportunities within ... the Medical Excellence & Operations team within Global Medical Affairs . This role is responsible for overseeing 3 medical...+ Serve as a key point of contact for senior leadership, providing updates, insights, and recommendations on strategic… more
- J&J Family of Companies (Spring House, PA)
- …at https://www.jnj.com/innovative-medicine We are searching for the best talent for a ** Senior Manager/ Associate Director** , ** Regulatory Medical Writing** ... meetings). + Maintaining and disseminating knowledge of industry, company, and regulatory guidelines. + Interacting with senior cross-functional colleagues and… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- …development programs. + Build professional network with key stakeholders outside of Global Regulatory Affairs to identify regulatory intelligence needs and ... The Associate Director of Regulatory Intelligence leads...technical discipline preferred. + Minimum of 5 years of regulatory affairs experience. + Minimum 2-3 years'… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- …accurate, evidence-based, and compliant with internal policies and external regulatory requirements. + Collaborate cross-functionally with Medical Affairs , ... The Associate Director, Scientific Communications manages the execution of...consistency, and compliance. This position reports directly to the Senior Director, CNS Medical Communications Lead. **Job Description** **Key… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- …statistical sections. + Discusses strategies with Global Clinical Development and Regulatory Affairs regarding study design and complex analysis issues, ... team and key stakeholders across different functional areas such as clinical, regulatory affairs , asset management, safety and clinical operation. + Familiar… more
- Merck (Upper Gwynedd, PA)
- …Office (PMO); and Administrative Professionals. **Position Description/Summary:** The GPAM Associate Director, Value & Implementation Project Manager (VIPM), is a ... to progress the R&D pipeline and realize its full potential. The Associate Director is expected to provide project management leadership and drive cross-functional… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- …cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to ... ** Associate Director, Small Molecule Analytical Development** + Lead...and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and implement stability study protocols… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Tax Attorney ( Associate General Counsel) Job Profile Title Associate General Counsel Job ... investment taxation, and will be comfortable navigating the nuanced regulatory frameworks applicable to mission-driven institutions with sophisticated investment… more
- J&J Family of Companies (Spring House, PA)
- …biomarker discovery, translational research, computer vision, clinical development, medical affairs , diagnostics, regulatory , and commercial teams to assess ... https://www.jnj.com/innovative-medicine Johnson & Johnson Innovative Medicine is recruiting an ** Associate Director, Oncology AI Biomarkers & Diagnostics** to join… more
- University of Pennsylvania (Philadelphia, PA)
- …(OCR) in the Perelman School of Medicine and reports directly to the Associate Director, PSOM Office of Clinical Research Compliance. The Clinical Quality Specialist ... University of Pennsylvania. The Clinical Research Quality Specialist will work with senior team members to facilitate and conduct high quality compliance reviews,… more
