- Merck & Co. (North Wales, PA)
- … Scientist ) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our ... Oncology (and/or Hematology)Prior experience in breast cancer idealPrior specific experience in clinical research and prior publication is desirable but not… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory strategy for their ... point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS.Develops worldwide product regulatory strategy… more
- J&J Family of Companies (Horsham, PA)
- Director , Clinical Research Scientist (Oncology) - 2406202641W **Description** Johnson & Johnson Innovative Medicine is recruiting for a Director , ... people can reach their potential. At Johnson & Johnson, we all belong. The Clinical Research Scientist works in the US Medical Affairs Solid Tumor group and… more
- Merck (North Wales, PA)
- **Job Description** **Position Description:** **Associate Director , Clinical Scientist ** This position drives scientific planning, strategy and execution of ... clinical protocol(s). + Serves as the lead clinical scientist on the clinical ...clinical data/medical protocol deviations in collaboration with the Clinical Director . + Builds talent and capabilities… more
- Merck (North Wales, PA)
- …Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new or marketed oncology medicines. Our ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will...percent of the time to manage future or ongoing clinical research projects. Qualifications **Education** + MD… more
- Merck (North Wales, PA)
- **Job Description** Under the guidance of a senior leader, the Principal Scientist , Outcomes Research -Women's Cancer has primary responsibility for developing ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses,… more
- Merck (North Wales, PA)
- … Scientist ) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage...preferred but not mandatory + Prior specific experience in clinical research and prior publication is desirable… 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 ... our strategic priorities. **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs Liaison is responsible for development and… more
- CSL Behring (King Of Prussia, PA)
- …used to treat serious and often rare conditions. Could you be our next Principal Clinical Scientist ? You will be hybrid in our King of Prussia PA, Marburg ... Germany or Bern Switzerland office. You will report to the Director of Global Clinical Science Lead. **Responsibilities:** + You will be responsible for… more
- Merck (West Point, PA)
- …of novel therapeutics, working in close collaboration with Discovery Sciences and late-stage Clinical Research . We work with all therapeutic areas within our ... colleagues in Translational Medicine, as well as Discovery Sciences and late-stage Clinical Research while developing and expanding your career. **Primary… more
- Organon & Co. (Plymouth Meeting, PA)
- …Director in Organon Regulatory CMC New Products, the Associate Principal Scientist (Associate Director ) is responsible for Regulatory Chemistry Manufacturing ... & Controls (CMC) aspects of clinical phase through market product registration for the assigned...development products and commercially approved compounds. The Associate Principal Scientist may also support project team goals and organizational… more
- Organon & Co. (Plymouth Meeting, PA)
- …Regulatory Chemistry, Manufacturing and Controls New Products, the Associate Principal Scientist (Associate Director ) is responsible for Regulatory Chemistry, ... Manufacturing and Controls (CMC) aspects of clinical phase through market product registration for the assigned biological/ biosimilar/small molecule products in… more
- Merck (West Point, PA)
- **Job Description** **Position Description:** **Associate Scientist , Cell Culture and Fermentation Sciences** As part of Our Company's Manufacturing Division, within ... Under the general scientific and administrative direction of the Director of Bioprocess Drug Substance Commercialization (BDSC) Cell Culture Fermentation… more
- J&J Family of Companies (Spring House, PA)
- Senior Director , R&D Data Science and Digital Health, Real-World Evidence and Advanced Analytics - 2406217069W **Description** Johnson & Johnson Innovative Medicine ... Medicine develops treatments that improve the health of people worldwide. Research and development areas encompass oncology, cardiovascular and metabolic disorders,… more
- Merck (North Wales, PA)
- **Job Description** The Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory strategy for their ... point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS. + Develops worldwide product regulatory… more
- Pfizer (Collegeville, PA)
- **ROLE SUMMARY** The Late-Stage Clinical Scientist (non-MD, Director ) is responsible for scientific oversight, data integrity and quality of clinical ... **QUALIFICATIONS** + Science degree (PhD, PharmD, or equivalent) and minimum of 7-year Clinical Research experience in industry/CRO, OR BA/BS and minimum of… more
