The Senior Director, Medical Affairs will provide global medical leadership for the R&D function of the Fresenius Kabi MedTech business, which includes medical devices and solutions associated with transfusion, cell therapies, and infusion technology. Participate in and guide risk management inputs for development projects, support definition and execution of clinical dev

include assisting the Center for Environmental Studies co directors, staff and RVCC administration with all aspects of project implementation, including Coordinating with community partners Collection of soil and vegetation field data Training and coordination of student interns Data entry, analysis, and reporting Creating and updating outreach content in web, print and ot

Leads multidisciplinary teams in delivering on the design, execution, strategy and management of various development, clinical pharmacology and regulatory engagements, from early translation to late development. Works collaboratively with and leads Certara team members and clients to develop clinical pharmacology and quantitative program strategies that are fit for purpos

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. The Sr. Medical Director will lead the development and execution of the medical strategy for Rett Syndrome. This will be accomplished by working in close collaboration with colleagues in Commercial, Regulatory, Market Acc

Tris Pharma, Inc. (www.trispharma.com) is a leading privately owned biopharmaceutical company in the U.S. with a focus on development and commercialization of innovative medicines that address unmet patient needs. We have more than 150 US and International patents including applications and have marketed several branded and generic products in the U.S., have licensed our

To accept primary responsibility for the provision of clinical and distributive pharmaceutical services. EDUCATION B.S. or PharmD. in Pharmacy, New Jersey Pharmacist license. EXPERIENCE One year experience in hospital pharmacy preferred. Basic knowledge and experience with unit dose dispensing system and i.v. admixture programs. Knowledge of clean room and compounding che

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. This position will serve as a technology partner in the Research and Development (R&D) and Technology Development & Operations (TD&O) domains, providing technology leadership, operational support and project management fo

Review every medication order and dosage for completeness, safety and efficacy prior to dispensing to an individual patient including routine, stat and investigational orders. Maintain drug information, investigational, educational, cost containment and clinical programs Experience Required Hospital pharmacy experience (or clinically relevant experience) or graduate of a

Pharmacist Per Diem Job ID 287253 Location US NJ Rochelle Park Experience (Years) 1 Category Healthcare Practitioners and Technicians Other Healthcare Practitioners and Technicians Street Address 96 Parkway Company Select Specialty Hospital NE NJ Rochelle Park Position Type Per Diem Overview Select Specialty Hospital Critical Illness Recovery Hospital Rochelle Park, New J

Prepares medication orders by compounding or admixing medications under supervision of a registered pharmacist. Checks all orders for completeness of information. Verifies patient information and proper physician authorization. Checks all orders for insurance approval before admixing. Under a professional's supervision, admixes drugs as ordered by physician in an accurate

Lead clinical pharmacology activities related to study design, protocol development, study execution, reporting and interpretation of data. Conduct PK and PK/PD analysis . Work closely with pharmacometrics team members and provides input related to analysis and reporting of PK and PK/PD. Lead development of clinical pharmacology sections for regulatory filings including a

Review every medication order and dosage for completeness, safety and efficacy prior to dispensing to an individual patient including routine, stat and investigational orders. Maintain drug information, investigational, educational, cost containment and clinical programs Experience Required Hospital pharmacy experience (or clinically relevant experience) or graduate of a

The Senior Manager, Regulatory Affairs position will support the Regulatory Affairs (RA) Director to help define the regulatory strategy for our innovative next generation technology for cellular therapy. This position will play a substantial role researching regulations, defining and implementing the regulatory strategy and engaging with health authorities to effectively

BioMed Tech I Facility PHS Bio Medical Services Location US NJ Denville ID 2024 160868 Category Non Clinical Tech Position Type Full Time Shift Days Job Type Non Exempt Overview Join our team of dedicated professionals who provide services and operational support to award winning hospitals through roles in supply chain, IT and cybersecurity, clinical engineering, capital

Singular talents thrive as an Associate Director of Medical Writing with Caudex. We advocate. We captivate. We cogently demonstrate. We combine gravitas with that lightness of touch that only comes from genuine, deeply held mastery and passion. We're recognised leaders in our field because we make the extraordinary seem effortless. We are your people. You're a recognised,