- Sevita (Philadelphia, PA)
- …today, and experience a career well lived. Operations Management Program Director /Program Specialist - Northeast, Philadelphia Starting Salary $53,500 Looking for ... and leadership skills to a team-based workplace that puts people first. As Program Director , you will be responsible for the operational management of an Adult Day… more
- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionGRACS CMC - Associate Principal Scientist, CMC, R4 - Pharm Pre-approval Reporting to the Sr Director / Director /Principal Scientist/Sr Principal ... Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our company's pharmaceutical pipeline products in accordance… more
- Merck & Co. (North Wales, PA)
- Job DescriptionAssociate Director , Business System Labeling Management Required experience and skills: Min. 5-10 years of experience with Pharmaceutical ... Regulatory Affairs Operations with Labeling Process and/or Digital Enablement...soon as possible.Job Description: Seeking a full-time Business System Associate for the Labeling Operations area within the GRACS… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist/ Associate Director , has primary responsibility for ... The incumbent is expected to work cross-functionally with clinical development, medical affairs, biostatistics, market access, commercial and country affiliates. The… more
- Merck & Co. (North Wales, PA)
- …engagements. This includes the ability to:--Strong knowledge of clinical research regulatory requirements (eg, GCP and ICH) Proven ability to manage competing ... +9 years of pharmaceutical, clinical drug development, project management, and/or medical field experienceOR Master's Degree +6 year of pharmaceutical, clinical drug… more
- Eisai, Inc (Exton, PA)
- …Quality Control, Regulatory , and CMC Program Management departments.The Associate Director of Biologics Operations maintains knowledge of established ... At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides...your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and… more
- Organon (Plymouth Meeting, PA)
- …The Position The Associate Principal Scientist ( Associate Director ) is responsible for developing and implementing Regulatory Chemistry, Manufacturing ... in accordance with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and submission of CMC… more
- J&J Family of Companies (Spring House, PA)
- …and if approved by the Company. **We are searching for the best talent for Associate Director , Regulatory Medical Writing - Oncology.** **Purpose:** + ... experience is required. + At least 8 years of relevant clinical/ regulatory medical writing experience is required. + Experience in project management and… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** The Associate Director , Global Regulatory Lead (GRL), reporting to the Executive Director , Senior Director or ... projects in their assigned therapeutic area portfolio. **Responsibilities** The Associate Director will be responsible to: + Develop regulatory strategy for… more
- Humana (Trenton, NJ)
- …the candidate will be required to work in either Central or Eastern Time. Associate Director , Regulatory Intake Compliance is responsible for enterprise-wide ... operational value and reduces compliance risk exposure for the organization. The Associate Director , Regulatory Intake Compliance will be responsible… more
- Merck (Upper Gwynedd, PA)
- **Job Description** GRACS CMC - Associate Principal Scientist, CMC, R4 - Pharm Pre-approval Reporting to the Sr Director / Director /Principal Scientist/Sr ... Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our company's pharmaceutical pipeline products in accordance… more
- Merck (North Wales, PA)
- **Job Description** ** Associate Director , Business System Labeling Management** **Required experience and skills:** + Min. 5-10 years of experience with ... Pharmaceutical Regulatory Affairs Operations with Labeling Process and/or Digital Enablement...as possible. **Job Description:** Seeking a full-time Business System Associate for the Labeling Operations area within the GRACS… more
- United Therapeutics (Trenton, NJ)
- …like lungs, pancreases and hearts. **Who you are** We are looking for a regulatory strategist who will advise on regulatory pathways, managing documentation and ... timelines, and supporting the preparation and execution of regulatory submissions for our whole organ tissue engineering program. Are you looking to fundamentally… more
- University of Pennsylvania (Philadelphia, PA)
- …and wellness programs and resources, and much more. Posted Job Title Assistant/ Associate Director , Grant and Contract Financial Administration Job Profile Title ... Associate Director D, Business and Finance, Research...stakeholders, research administrators, internal and external partners, sponsors, and regulatory agencies throughout the post award lifespan of a… more
- Sumitomo Pharma (Trenton, NJ)
- …currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Medical Director .** The Associate Medical ... for SMPA investigational and commercial products. The incumbent will provide medical safety support for safety signal management throughout product lifecycle… more
- Merck (West Point, PA)
- …Manufacturing Operations, Drug Delivery Systems and Devices within our Manufacturing Division ( Associate Director ). This role serves as a Virtual Plant Manager ... contact for all dealings between our Company and the External Partner, the Associate Director External Manufacturing Operations is accountable for establishing a… more
- Merck (West Point, PA)
- …in West Point, PA / Rahway, NJ is seeking a curious and collaborative Associate Director to support our robust infectious disease and vaccines pipeline. As ... an Associate Director , you will represent QP2 on...vendors and partners, creating an aligned, quantitative and model-informed regulatory framework to impact strategies and decisions of drug… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Position Summary:** The Associate Director of Global Medical Affairs Omnichannel will be responsible for developing and leading the omnichannel strategy ... + **Compliance & Governance:** + Ensure all omnichannel activities adhere to internal medical , legal, and regulatory standards. + Collaborate with Compliance and… more
- Merck (West Point, PA)
- …component of decision-making at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This ... development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an...Associate Director will work with scientists within… more
- Merck (West Point, PA)
- **Job Description** The Associate Director of Laboratory Quality Assurance within the Quality Assurance Center of Excellence is responsible for providing Quality ... deployment of WP Site and our Company Manufacturing Division priorities. The Associate Director drives quality improvement activities and ensures alignment… more
