- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … clinical or basic research in a Pharmaceutical company, a Medical device /Diagnostic company, Academic Research Organization (ARO) or Contract Research ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions in… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …requirements. This position has experience working on Phase I-IV studies within the medical device and/or pharmaceutical industry within one or more therapeutic ... more years data management and/or related industry work experience in a medical device , pharmaceutical company, or similar environment (eg, CRO) required.Daiichi… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … clinical or basic research in a Pharmaceutical company, a Medical device /Diagnostic company, Academic Research Organization (ARO) or Contract Research ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … clinical or basic research in a pharmaceutical company, a medical device /Diagnostic company, Academic Research Organization (ARO) or Contract Research ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … clinical or basic research in a Pharmaceutical company, a Medical device /Diagnostic company, Academic Research Organization (ARO) or Contract Research ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …that support the clinical development and regulatory requirements of a clinical program. Relationships The Senior Medical Writer reports to a Director ... relationships with global and local cross-functional study teams, including personnel from Medical & Science, Clinical Pharmacology, Biostatistics, Clinical … more
- Merck & Co. (North Wales, PA)
- …includes, but is not limited to: Reporting to Senior Management of the Medical Device and Combination Product (MDCP) Quality Assurance Operations team, the ... and maintenance of technical business solutions, reviewing and approving medical device /combination product documentation to support regulatory filings… more
- Eisai, Inc (Nutley, NJ)
- …must include two or more of the following areas: infusion, diagnostic, biologic, medical device , buy and bill, rare disease, specialty pharmacy, and/or ... record of internal success is required. A combination of infusion, diagnostic, biologic, medical device , buy and bill, rare disease, or specialty pharmacy… more
- Merck & Co. (Rahway, NJ)
- …Preferred Experience: Product management experience with regulated Software as a Medical Device (SaMD), and/or Digital Pathology Experience commercializing and ... and/or healthcare space Understanding and experience with global regulatory requirements for Medical Device and/or AI algorithms Budget management and approval… more
- Merck & Co. (Rahway, NJ)
- …regulatory activities with cross- product or cross-functional impact, including drug device /combination products and software-as- medical device platforms.- ... to the mission and vision of the Global Regulatory Affairs and Clinical Safety (GRACS) function of our company's Research & Development Division by:Developing… more
- Merck & Co. (Rahway, NJ)
- …Our Research Laboratories to ensure cross functional alignment through clinical development and successful commercial implementation. Close collaboration with ... across our Company functions as well as external partners (diagnostic & device technology companies, reference laboratories, etc.) is fundamental to the success of… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Team, Safety Management Team, Clinical Safety and Pharmacovigilance Medical Affairs, Companion Diagnostics/ Device Laboratories Vendors/ CROs Leadership/ ... and key business function and collaborate with RD and Medical Affairs Quality to provide clinical safety QA advise wherever necessary. Ensure requirements are in… more
- Lundbeck (Omaha, NE)
- …from an accredited college or university 4+ years pharmaceutical, biopharmaceutical, biologics, medical device sales or related healthcare sales experience Must ... Skilled Nursing Facilities.You will drive demand creation by providing comprehensive clinical knowledge, executing sales and marketing strategies in the local… more
- Catalent (MA)
- …Candidate Minimum of 3 years of sales experience in the bio, pharma, medical device industries, or other related industriesExperience in developing and ... services with a particular focus on identifying and closing GLP clinical and commercial related opportunities. Other responsibilities for the Account Director,… more
- Lundbeck (Dallas, TX)
- …5+ years of Specialty Sales experience in Pharmaceutical, Biopharmaceutical, Biologics or Medical Device sales experience Ownership and accountability for the ... of our infusion product, driving demand creation by providing comprehensive clinical knowledge, executing sales and marketing strategies in the local market… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and/or post marketing in Clinical research, Pharmaceutical company, CRO or Medical Device setting preferred- 4 or More Years Experience in oncology ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Catalent (St. Petersburg, FL)
- …years auditing experience Experience working in an auditing role within the Pharmaceutical/ Medical Device industry, required Knowledge and understanding of the ... ISO, and related International Regulations affecting pharmaceutical products and medical devices Sterile/biologic/ATMP/C> auditing experience preferable Working knowledge of… more
- Catalent (St. Petersburg, FL)
- …experience , required Experience working in an auditing role within the Pharmaceutical/ Medical Device industry Knowledge and understanding of the following ... (FDA), ISO, and related International Regulations affecting pharmaceutical products and medical devices Working knowledge of industry related guidelines such as ICH… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …responsible related experience; including hands on related pharmaceutical or medical device /pharmaceutical combination product experience and actual regulatory ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and/or post marketing in clinical research, pharmaceutical, CRO or medical device setting required- Experience within oncology therapeutic area and/or ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...as well as strong technical skills in working with ( clinical ) data. The position holder will require strong skills… more
