- GE HealthCare (Waukesha, WI)
- …working in the medical technology, medical device, or pharmaceutical industry in Medical or Clinical Affairs roles + MBA or Masters degree in business related ... between business leaders and research team to define bench and human clinical research priorities for product development, regulatory submissions, and marketing,… more
- Edwards Lifesciences (Naperville, IL)
- …product briefings for cross functional teams such as complaints, Engineering, regulatory affairs , quality affairs and clinical affairs + Regularly ... **Sr. Director , Global Professional Education, Training - IHFM** Many...the IHFM Institute (HCPs) and IHFM University (Commercial Reps, Clinical ) brands by executing an education curriculum comprised of… more
- Houston Methodist (Houston, TX)
- …and the International Conference on Harmonization (ICH). This position communicates with regulatory affairs office for FDA submissions across multiple studies of ... - REQUIRED** + N/A **LICENSES AND CERTIFICATIONS - PREFERRED** + RAC - Regulatory Affairs Certifications (RAPS) **OR** + CCRC - Certified Clinical… more
- Astrix Technology (Boston, MA)
- …FDA, EMA, and ICH guidelines. + Collaborate with cross-functional teams, including preclinical, clinical operations, and regulatory affairs , to integrate and ... **Senior Medical Director ** Clinical Boston, MA, MA, US...RNA-targeted therapeutic programs worldwide. + Ensure adherence to international clinical development and regulatory standards. **Qualifications:** +… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …Regeneron's drug development pipeline in partnership with Diagnostic Strategy Leads and IVD Regulatory Affairs . This is a leadership role within Regeneron's ... Develop and maintain project plans to closely track CDx development and CDx regulatory activities against clinical drug development and study timelines + Review… more
- AmeriHealth Caritas (Philadelphia, PA)
- …Medical Director (s), Utilization Management and the Vice President, Medical Affairs . ;The following responsibilities are in regard to enrollees with medical ... as it relates to health management. + Maintains compliance with applicable regulatory guidelines, AmeriHealth Caritas clinical policies and procedures, and… more
- Chiesi (Boston, MA)
- …trends into impactful narratives for global stakeholders. + Partner with R&D, clinical development, regulatory , and commercial teams to ensure seamless, ... and rewarding work. Who we are looking for Purpose As the Senior Director , Global Scientific Engagement and Innovation, you will spearhead the strategy, development,… more
- Bristol Myers Squibb (Princeton, NJ)
- …(Masters, PhD, PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** ... in their personal lives. Read more: careers.bms.com/working-with-us . **Associate Director , Global Regulatory Strategy, Neuroscience** **Position Summary:** The… more
- State of Minnesota (Preston, MN)
- …of residents. The DON works closely with the Home Administrator to ensure clinical services meet regulatory requirements and agency standards of practice. The ... Nurse (RN) Administrative Supervisor** **Agency: Minnesota Department of Veterans Affairs ** + **Job ID** : 88695 + **Location** :...DON also works with the home's Medical Director and community-based providers to ensure clinical … more
- Sanofi Group (Cambridge, MA)
- …patient advocacy associations, clinical development, Global Medical Leadership, Regulatory , Medical Affairs , Product Communications, and lead agency ... **Job Title:** Global Director Market Development and Strategy - Sickle Cell...customer-validated Rilzabrutinib disease and science story in partnership with Clinical Development and Global Medical Affairs . +… more