- Merck & Co. (North Wales, PA)
- …for world-wide regulatory application submissions of drug and vaccine clinical development projects.Be accountable for submission data standards planning activities, ... keeping current with industry submission data standards including SDTM, ADaM, clinical site data for CDER inspection planning, etc.Responsible for continuous… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Chemical Biotechnologies group within the Process Research & Development Enabling Technologies Department in Rahway, New Jersey is seeking a ... improved functions and properties to enable drug discovery and impact clinical supply and commercial manufacturing processes.- They will give scientific… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately...and Boston metro areas, with additional growth in the Research Triangle (NC) and San Francisco Bay Area. Please… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately...and Boston metro areas, with additional growth in the Research Triangle (NC) and San Francisco Bay Area. Please… more
- Merck & Co. (Biloxi, MS)
- …bulletins.Assist in the design, execution, and analysis of field trials and clinical studies for new or existing products.Establish and maintain relationships with ... customer needs through various channels and provide feedback to prioritize research and development needs.Aid in development of technical and marketing brochures… more
- Merck & Co. (Rahway, NJ)
- …and execute design verification strategies that successfully supports the clinical instruction(s) and commercial market approval(s) of combination products.Principal ... strategies for assigned drug-device combination product program(s) for successful clinical introduction(s) and commercial market(s) approval(s).Define design input(s)/ output(s)… more
- Legend Biotech USA, Inc. (Philadelphia, PA)
- …will play a pivotal role in guiding toxicology strategy from early research through IND-enabling studies and into clinical development, ensuring regulatory ... seeking Sr. Director of Toxicology as part of the Clinical Development team based in Philadelphia, PA or Somerset,...the employee or the company. Legend may adjust base salary or other discretionary compensation at any time based… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary The Executive ... disciplines and cultures. Additionally, he/she will possess advanced knowledge of clinical operations and relevant regulatory requirements. The individual will have… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. SummaryUS Medical Affairs ... under the supervision and leadership of the Executive Director of Medical Research and Strategy, US Oncology Medical Affairs (USOMA). Develops the USOMA strategy… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately...a commutable distance or are willing to relocate.Compensation:The target salary range for this role is: $80,000 - $95,000.… more
