- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position?** Reporting to the Director in Organon Regulatory CMC,?the Associate Principal Scientist is responsible for?developing ... 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)
- …**The Position** 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… more
- Organon & Co. (Plymouth Meeting, PA)
- …authoring and review of Investigator Brochures, INDs, briefing books and other regulatory documents, as applicable. The Associate Director, Biopharmaceutics will ... **Job Description** **The Position** The Associate Director, Biopharmaceutics will provide expert biopharmaceutical guidance on the pharmacokinetic performance of… 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 ... priorities. Developing and implementing patient-centered endpoints strategies, working with regulatory , Value Strategy Assessment (VSA's) and contracting. The role… 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 for ethical...our business. + Maintain a vigilant watch over the regulatory environment specific to Primary Market Research and Data… 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 provide ... in R&D functions (eg, Clinical Research, Early Development, Medical Affairs, Pharmacovigilance, Regulatory Affairs, etc.) + At least three years of experience in… more
- Teleflex (Philadelphia, PA)
- Associate Sales Representative, Trauma and Emergency Medicine - Philadelphia, PA **Date:** Nov 21, 2025 **Location:** Philadelphia, PA, US **Company:** Teleflex ... sales process across Teleflex's trauma and emergency medicine portfolios. The Associate Sales Representative (ASR) will assist territory managers and sales… 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 ... decisions + A deep understanding of the pharmaceutical industry, including regulatory requirements, market dynamics, and emerging AI technologies, with the foresight… more
- CSL Behring (King Of Prussia, PA)
- …trackers, SOPs, and governance frameworks that ensure scientific integrity and regulatory compliance. You will also drive innovation in publication metrics and ... digital engagement, helping us measure and enhance our scientific impact globally. As a more senior member of the publications team, you will also be expected to provide strategic and operational mentorship to less experienced colleagues. **RESPONSIBILITIES… more
- CSL Behring (King Of Prussia, PA)
- …of biotech/pharmaceutical experience. **Experience** + Strong knowledge of the regulatory requirements for MDRP, Medicare/IRA, Veteran's Healthcare Act, and other ... Federal regulations mandating price and/or transparency disclosures. + Experience with implementation and utilization of financial & pricing systems. Model N preferred. + Strong Excel skills as well as MS Office proficiency Demonstrated ability to function… more
- Parexel (Trenton, NJ)
- Parexel FSP has an exciting opportunity in Site Start Up! The Associate Manager, Site Start Up will have responsibilities for the creation and management of Site ... Working knowledge of the clinical drug development process, ICH/GCP and regulatory guidelines/directives - Demonstrates ability to prioritize and manage multiple… more
- ABBTECH Professional Resources, Inc. (Trenton, NJ)
- **Financial Project Associate ** **Exempt** Embark on a dynamic career with Premier Group Services, Inc., a leading CPA Management and Consulting firm dedicated to ... approach that ensures responsiveness and lasting relationships. **Join as a Project Associate ** As a Project associate at Premier Group Services, Inc.,… more
- Parexel (Trenton, NJ)
- …we are expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global Immunology and Inflammation ... Therapeutic Franchise. As an Associate / Medical Director, you will work closely with...including medical review of serious adverse events. - Support regulatory safety reporting activities - Ensure client needs and… more
- Towne Park (Plymouth Meeting, PA)
- …best practices for data integrity, system security, and compliance with regulatory requirements. + Lead projects related to system upgrades, enhancements, and ... _described here are representative of those that must be met by an associate to_ **_successfully perform the essential functions of this job_** _. Reasonable… more
- BeOne Medicines (Pennington, NJ)
- …+ Manage and coordinate global change ensuring stakeholders alignment. Assist in Regulatory filings and Health Authority site inspections to license and maintain ... and lifecycle process improvements. + Working knowledge of GMP and regulatory requirements of biopharmaceutical manufacturing. + Ability to work both independently… more
- Parexel (Trenton, NJ)
- …readiness for First Subject First Visit (FSFV) + Partners with Clinical Research Associate (CRA) to ensure site monitoring readiness in anticipation of FSFV + ... with CRA for enrollment delivery during study conduct + Partners with local Regulatory authorities and Study Start up teams to ensure timely completion on country… more
- Globus Medical, Inc. (Audubon, PA)
- …can resume their lives as quickly as possible. **Position Summary** **:** The Regulatory Affairs Associate assists in drafting, submitting and gaining clearance ... for IDE and PMA reporting + Reviewing Document Change Orders for Regulatory compliance, including drawings and labeling changes + Performing routine maintenance of… more
- Coinbase (Trenton, NJ)
- …management processes. *What you'll be doing (ie. job duties):* * The Senior Associate of Regulatory Change Management (RCM) will support the management, ... and alignment. Attendance is expected and fully supported. The Coinbase Regulatory Change Management (RCM) function is responsible for the development, execution… more
- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Associate Director, Regulatory Job Profile Title Associate Director, Clinical ... Description Summary With the oversight of the Director, the Associate Director for Regulatory Affairs will oversee the portfolio of clinical research undertaken… more
- Sumitomo Pharma (Trenton, NJ)
- …a dynamic, highly motivated, and experienced individual for the position of ** Associate Director, Regulatory Affairs (Oncology).** The Associate Director ... the US. He/She will primarily function as a regional regulatory leader (RRL) and/or Global Regulatory Leader...a regional regulatory leader (RRL) and/or Global Regulatory Leader (GRL) for assigned products. This position is… more
