- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** The Associate Principal Scientist is responsible for developing and implementing Regulatory CMC strategies for assigned ... products in accordance with global regulations and guidance's, and Company procedures. The Associate Principal Scientist will lead the preparation and… more
- Merck (North Wales, PA)
- **Job Description** **Description:** The Associate Principal Scientist , Oncology Publications Medical Writing, works with scientists in our company's ... select early-stage development projects and our company's science. The Associate Principal Scientist is expected...key issues for publications, define hypotheses and sources of data , and review data analysis plans. **Primary… more
- J&J Family of Companies (Spring House, PA)
- Associate Director/ Principal Scientist Cell Line Engineering - 2406177894W **Description** At the Johnson & Johnson Innovative Medicines, we are working to ... cell and pathway engineering, assay development, and large scale data analysis & visualization. + Proficiency in CHO cell...Joining our team as a cell engineering leader and scientist specializing in CHO cell expression offers an exciting… more
- Merck (North Wales, PA)
- …we collaborate to discover the next medical breakthrough. **Position Description:** The Associate Principal Scientist Statistical Programming leads the ... standards that optimize analysis and reporting and promote a strategic knowledge-base data model, + maintaining and managing a project plan including resource… more
- Merck (North Wales, PA)
- …and global human health. The incumbent is responsible for statistical planning and data analysis of Phase I/II oncology clinical trials as well as translational ... projects and studies. + Interact with Clinical, Regulatory, Statistical Programming, Data Management, and other company Research Laboratories scientists in designing… more
- Merck (North Wales, PA)
- …experience in developing analysis and reporting deliverables for R&D projects ( data , analyses, tables, graphics, listings) + Strong project management skills; ... + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise. + Experience… more
- Pfizer (Collegeville, PA)
- …Consistent with the SSRP, performs and documents regular review of individual subject safety data , and performs review of cumulative safety data with the safety ... monitor may delegate these responsibilities to the study clinician scientist identified in the SSRP. The specific components of...identified in the SSRP. The specific components of safety data review are detailed in the appropriate SOPs and… more