- Rhythm Pharmaceuticals (Boston, MA)
- …our tenacity to overcome barriers, together. Opportunity Overview The National Account Director (NAD) will be a field-based strategic leader responsible for driving ... all payer channels + Partner cross-functionally with Patient Services, Marketing, Medical Affairs, and Commercial Operations to develop integrated access strategies.… more
- Danaher Corporation (Fargo, ND)
- …and improve human health. We are seeking a strategic and technically accomplished Director of Drug Product CMC to lead client-facing drug product development and ... Master's degree in chemical engineering, chemistry, pharmaceutical sciences, or a related scientific discipline highly preferred . + Prefer 10+ years of experience… more
- Otsuka America Pharmaceutical Inc. (Augusta, ME)
- …skilled and experienced professional to join our organization as the Assoc. Director of Manufacturing Science and Technology (MSAT) for Upstream processes. This ... Responsibilities:** + Lead the upstream development, fostering a culture of scientific excellence, innovation, and continuous improvement + Serve as the primary… more
- Otsuka America Pharmaceutical Inc. (Concord, NH)
- **Position Overview:** The Senior Director , MSAT Biologics provides strategic and technical leadership for all late-stage and commercial manufacturing processes for ... lead, mentor, and manage the MSAT team, fostering a culture of scientific excellence, collaboration, and accountability. + Provide senior technical leadership and… more
- University of North Carolina- Chapel Hill (Chapel Hill, NC)
- …Range: Dependent on Qualifications/Experience Position Summary/Description: We are seeking the Associate Director for Population Science (AD for Pop Sci) at the UNC ... qualifications. The AD for Pop Sci is both the scientific and administrative leader for fostering bi-directional communication and...they are physically located in the center of the medical campus in the UNC Lineberger building, a 79,000… more
- Bristol Myers Squibb (Cambridge, MA)
- …focus is in a specific disease area / indication and will ensure scientific and technical excellence of clinical development programs and deliverables + This ... + Will work closely with colleagues in BMS Research, Development, Regulatory, Medical , Commercial and other key functional areas on a global basis; additionally… more
- Pfizer (Cambridge, MA)
- …appropriate local and global discussions. * Produces and presents quality scientific contributions at external meetings and for publication. * Responsible for ... software tools and colleagues are best in class. Produce and present quality scientific papers at external meetings and for publication. * Prepares and delivers… more
- GRAIL (Menlo Park, CA)
- …up-to-date knowledge of applicable regulatory requirements and relevant scientific /technical developments. + Identify regulatory risks and propose alternative ... development, clinical affairs, quality, or program management within the IVD, medical device, or pharmaceutical industries. + Regulatory affairs and IVD device… more
- ChenMed (Louisville, KY)
- …The responsibilities include but are not limited to: geriatric assessment, medical history, physical exam, diagnosis and treatment, development of the plan ... care professionals. The PCP will consult with the applicable managers and medical directors to ensure compliance with guidelines along with participating in risk… more
- AbbVie (North Chicago, IL)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... ensure consistent preparation of CMC regulatory submission documents of high scientific and technical quality that are compliant with global regulatory requirements.… more