- Merck (West Point, PA)
- **Job Description** **Position Description:** ** Director , Quantitative Pharmacology and Pharmacometrics Immunology (R5)** The Quantitative Pharmacology and ... Pharmacometrics (QP2) Department of our Research & Development Division in West Point, PA /.../ Rahway, NJ is seeking a curious and collaborative Director to support our rapidly expanding immunology … more
- CSL Behring (King Of Prussia, PA)
- …and answering key business questions globally, influencing Forecasting, Market Research , R&D and contributing to strategic decisions for various programs ... several TAs (including, but not limited to, Transplant & Immunology , Hematology). + Will support CI Lead to support...multiple disease states and therapy areas. + Experience with clinical data interpretation as well as competitive intelligence is… more
- Teva Pharmaceuticals (West Chester, PA)
- …least 5 years of relevant biopharmaceutical industry clinical development experience in immunology clinical research + Solid knowledge and experience of ... **How you'll spend your day** + Directing and implementing clinical research plans and programs according to...preferred + Demonstrated competence and track record at Study Director / Clinical Lead level + Experience with… more
- CSL Behring (King Of Prussia, PA)
- …market biotherapies used to treat serious and often rare conditions. Could you be our next Director Clinical Research ? This is a hybrid role located in our ... experience, with 1 including accountability for medical oversight/evaluation or clinical development. + Industry experience in designated therapeutic area(s). +… more
- System One (King Of Prussia, PA)
- Title: Executive Medical Director , Clinical Development - Late Phase Location: Remote 100% Type: Perm Start Date: ASAP Leading Pharmaceutical Company located in ... PA/NJ is hiring a Executive Medical Director , Clinical Development - Late Phase 5+...protocols, data collection systems and final reports. May recruit clinical investigators for research studies. Responsibilities also… more
- Merck (Upper Gwynedd, PA)
- **Job Description** We are seeking a Director (Principal Scientist), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can help ... advance our pipeline and drive our strategic priorities. The Director , Principal Scientist | Regulatory Affairs Liaison is responsible for development and… more
- Merck (North Wales, PA)
- **Job Description** We are seeking a Senior Director (Sr. Principal Scientist) Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can ... therapeutic area, with a specific focus on development programs in Immunology , Neuroscience and/or Ophthalmology. The individual functions with a high degree… more
- CSL Behring (King Of Prussia, PA)
- … research , development and manufacturing processes of pharmaceuticals (CMC, non- clinical , clinical , and regulatory).** **Expert level skillset in creating ... to treat serious and often rare conditions. Could you be our next Associate Director , R&D Project Planning Capability Lead? This position is located in our King of… more
- CSL Behring (King Of Prussia, PA)
- …in a health care environment, preferably pharmaceutical or other organization engaged in clinical research . + Familiarity with global clinical development ... **The Opportunity:** Reporting to the Director and Lead Counsel, Global Clinical ...more than 100 countries living with conditions in the immunology , hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic… more
- CSL Behring (King Of Prussia, PA)
- …Prussia PA, Marburg Germany or Bern Switzerland office. You will report to the Director of Global Clinical Science Lead. **Responsibilities:** + You will be ... often rare conditions. Could you be our next Principal Clinical Scientist? You will be hybrid in our King...biotechnology or pharmaceutical industry (or where relevant a biomedical research organization). + 5+ years managing projects. + In-depth… more
- CSL Behring (King Of Prussia, PA)
- …related disciplines. + Minimum of 5 years of professional work experience in clinical research in the Pharmaceutical Industry, minimum 4 years' experience in ... and implementation of the assigned Global R&D Quality Audit Program with focus on Clinical Development (from early First in Human to late clinical phases) in… more
- CSL Behring (King Of Prussia, PA)
- …role from others (2 - 3 sentences). The purpose of the position of Executive Director R&D Quality is to lead a dedicated team responsible for quality oversight for ... combination products regulations. Quality oversight is provided for toxicology studies, clinical development, clinical supply manufacture and packaging and… more