- Merck & Co. (North Wales, PA)
- …through interaction with key scientific leaders.Specifically, the Senior Principal Scientist is responsible for:Planning clinical trials (design, operational ... Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide...timely and equitable access to our medicines.The Senior Principal Scientist has primary responsibility for protocol development and medical/scientific… more
- Merck & Co. (North Wales, PA)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research activities ... compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development,… more
- Pfizer (Collegeville, PA)
- …the development team to establish, lead, coordinate, and execute the early oncology clinical development plan(s). You will lead the development of the clinical ... protocol and participate as an individual contributor on clinical teams with Pfizer development operations and the project team, to meet enrollment and study… more
- Merck & Co. (Upper Gwynedd, PA)
- …science of preclinical discovery into compounds ready for assessment in large clinical populations.We are seeking a highly qualified physician- scientist with a ... Job Description Senior Principal Scientist Translational Medicine, Immunology Translational Medicine in our...experience in the pharmaceutical industry and Immunology R&D and clinical and academic expertise in Immunology-related areas such as… more
- Merck & Co. (North Wales, PA)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Merck & Co. (North Wales, PA)
- …drug/vaccine projects in Late Development Statistics.Lead the interaction with Clinical , Regulatory, Statistical Programming, Data Management, and other Scientists ... from our Research & Development Division in designing and analyzing clinical trials, and in coordinating the statistical activities for clinical drug/vaccine… more
- Merck & Co. (North Wales, PA)
- …or related field plus 5 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences, ... or related field plus 3 years SAS programming experience in a clinical trial environment Department Required Skills and Experience: Excellent communication (oral,… more
- Merck & Co. (North Wales, PA)
- …This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.-The… more
- Eisai, Inc (Exton, PA)
- …proteins.Demonstrated knowledge of biopharmaceutical development through all clinical phases and post-commercialization.Strong familiarity with cGMP/ICH/FDA/EMA ... a must.Eisai Salary Transparency Language:The base salary range for the Scientist II, Analytical Outsource & Stability is from :113,400-148,900Under current… more
