Senior Principal Scientist, Thoracic Malignancies

Job SummaryMerck Sharp & Dohme (MSD) is seeking a highly skilled Principal Scientist to lead clinical research activities in gynecological malignancies. The successful candidate will be responsible for planning and directing clinical trials, managing research teams, and collaborating with cross-functional groups to advance the development of new oncology...

**Job Summary**Merck Sharp & Dohme is seeking a highly skilled Senior Principal Scientist to lead clinical research activities in oncology medicine development. The ideal candidate will have a strong background in clinical medicine and biomedical research, with a proven track record of scientific scholarship and achievement.**Key Responsibilities**Evaluate...

Job SummaryWe are seeking a highly skilled Senior Principal Scientist to lead our clinical research efforts in hematology and lymphoma. As a key member of our team, you will be responsible for planning and directing clinical research activities, including study design, placement, monitoring, analysis, and regulatory reporting.Key Responsibilities:Evaluate...

**Job Summary**The Principal Scientist/Director is responsible for developing and implementing Chemistry, Manufacturing, and Controls (CMC) regulatory strategies for our organization's biologics product franchises in accordance with domestic and international regulations and guidance.**Key Responsibilities**Lead the preparation and submission of CMC sections...

Job DescriptionEarly Device Program Strategy and Due Diligence Principal ScientistJob SummaryThe Principal Scientist of Early Device Program Monitoring & Due Diligence will play a pivotal role in leading and coordinating diverse activities between various device and combination product development, discovery, and formulation development teams.Key...

Job DescriptionMerck Sharp & Dohme (MSD) is seeking a highly skilled Principal Scientist, Clinical Research, Breast Cancer to join our team. As a key member of our clinical research team, you will be responsible for planning and directing clinical research activities involving new or marketed Oncology medicines.Key Responsibilities:Develop and execute...

Job DescriptionOur company is seeking a highly skilled Principal Scientist to join our Biologics Process Research & Development (BPR&D) team. As a key member of our team, you will be responsible for designing and developing innovative purification processes for biologics in early- and late-stage development.ResponsibilitiesCollaborate with cross-functional...

Job DescriptionPosition Title: Director/ Principal Scientist, Regulatory ComplianceDepartment: Device Quality & RegulatoryBrief Description of Position:This position will be part of the Device Quality & Regulatory Team within Global Regulatory Affairs and Clinical Safety (GRACS). The primary responsibility for this position is to ensure regulatory compliance...

Insight Global is looking for an Associate Principal Scientist, Global Regulatory Affairs CMC to join the Global R&D organization of a large pharmaceutical company. This individual will be responsible for assessing change controls while reviewing technical documentation and scientific information. The Associate Principal Scientist will spend the majority of...

Insight Global is looking for an Associate Principal Scientist, Global Regulatory Affairs CMC to join the Global R&D organization of a large pharmaceutical company. This individual will be responsible for assessing change controls while reviewing technical documentation and scientific information. The Associate Principal Scientist will spend the majority of...

The Associate Principal Scientist is responsible for developing CMC regulatory submission strategies and timelines for assigned pharmaceutical projects/products in accordance with global regulations and guidance. The Associate Principal Scientist is also responsible for the preparation and review of information required for development of regulatory CMC...

The Associate Principal Scientist is responsible for developing CMC regulatory submission strategies and timelines for assigned pharmaceutical projects/products in accordance with global regulations and guidance. The Associate Principal Scientist is also responsible for the preparation and review of information required for development of regulatory CMC...

We are seeking an experienced and motivated scientist/engineer to join the Biologics Downstream Operations team within Bio. Process Research and Development (BPRD). The successful candidate will be charged with operations leading downstream pilot pla Operations, Specialist, Operation, Processing, Senior, Manufacturing, Development