- Daiichi Sankyo, Inc. (Bernards, NJ)
- … trial and screen failures. Clinical trial protocol development and reviews ( clinical trial protocols and medical device protocols)ICF reviews to ensure ... of a CDx study/IVDR performance evaluation study integration of an assay into clinical testing (before testing) and once data is ready for CDx submission (after… more
- Merck & Co. (Rahway, NJ)
- …portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team ... opportunity is fast paced and contributes to the Pharmaceutical Sciences and Clinical Supplies (PSCS) deliverable which is the development of robust compositions,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. JOB SUMMARYThe Senior Director , Head Medical affairs Quality Assurance in Global RD/PV QA is accountable ... QA RDPVQA, and oversees multiple levels of direct reports (Directors, Associate Directors, Managers, contractors as applicable) across the Global Quality teams… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. JOB SUMMARY The Senior Director , Head Medical affairs Quality Assurance in Global RD/PV QA is accountable ... QA RDPVQA, and oversees multiple levels of direct reports (Directors, Associate Directors, Managers, contractors as applicable) across the Global Quality teams… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …academic translational clinical research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for Director and 6-9 years ... **Job Description** Otsuka is seeking a Director , Global Clinical Development (GCD), who...prior personnel management experience, will support position at entry ( Associate Director / Director ). + An advanced… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- **Job Description Summary** As Regulatory Affairs Associate Director , you will be responsible for leading RA team members involved in device project ... a strong and respected voice. + Comprehensive knowledge of US medical device regulations (FDA), Clinical Practice standards, Laboratory Practice regulations, and… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- … Clinical Expertise: Comprehensive understanding of regulatory requirements and clinical evidence generation methodologies in the medical device /diagnostics ... team in SM business unit, guiding compliance, product development, and clinical validation. **Key Responsibilities:** + Strategic Medical Leadership: Drive medical… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …best self. Become a **maker of possible** with us. **Position Overview:** The Associate Director of Marketing, Specimen Management Solutions is responsible for ... multiple collaborators within the US and Global platforms-including marketing, sales, clinical and medical affairs resources to ensure that short and long-term… more
- Bristol Myers Squibb (Princeton, NJ)
- …author of numerable SOPs, the Cyclotron Radiation Safety and Operations Manual, X-ray device use, and the laser safety procedures. + Oversee the Cyclotron facility ... Including specialized training for Cyclotron operators and radiochemists, x-ray device users, preclinical imaging, radiochemistry suite, medical staff, benchtop… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …worldwide business team, regional leadership in the Medical Affairs Function and the Associate Director of Medical Affairs in Specimen Acquisition to align and ... Reporting directly to the business unit Vice President of Medical Affairs, the Director of Medical Affairs has the responsibility to support the VP, Medical Affairs… more
