(Primary function) This position is responsible for providing pathology leadership and support across Discovery Biology, including Toxicology, Pharmacology and Translational Sciences. Essential Functions of the Job (Key responsibilities) Provide pathology support for studies across Discovery Biology, including guidance on study design, endpoints, sample collection and pro

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 Senior 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

The Senior Director, Medical Affairs, Parenteral Nutrition (PN) is a critical role as this individual serves as the lead for the US PN Medical Affairs team and is responsible for developing and executing the US Medical Affairs strategy. This individual also collaborates closely with the Global business unit (BU) and the regional marketing organization to identify US nutri

The Senior Director, Clinical Development Medical Affairs (CDMA) drives strategy and accountability for the hepatology drug program execution, ensuring alignment with brand team objectives, incorporation of relevant internal and external insights and the generation of an R&D plan that delivers for unmet patient need, generates competitive differentiation, and prepares for

include but are not limited to Provides development portfolio & program management to cross functional, cross divisional teams to drive execution and delivery in early to late phase complex development management programs to meet company strategic objectives. Actively manages cross program interdependencies and trade offs to ensure multiple programs are executed to predict

The primary responsibility of this position is to provide guidance to MSLs in cultivating current and future thought leaders in academic and clinical medicine at the local, regional, and national levels in the field of Hematology Oncology. The MSL Associate Director will lead, manage, coach, train, and develop MSL direct reports to support high performance, and to align w

(Primary function) The Associate Director, Clinical Trial Head is accountable for all aspects of assigned clinical trials/program. The Associate Director is responsible for program level activities as assigned and is accountable for the day to day clinical development operational plans in accordance with budget and timelines and with standard operating procedures (SOP), IC

Sets up, adjusts, operates, and calibrates laboratory equipment and instruments within the GC and/or GC MS laboratories. Troubleshoots instrument problems and performs general system maintenance and prepares analytical standards for various projects. Performs standard and routine analyses, analyzes data, and writes reports. Responsible for advanced sample preparation and

Responsible for creating a patient profile in the pharmacy information system. Enters necessary prescription plan information in the patient profile for processing and adjudicating patient's prescriptions. Responsible for entering all new patient prescription information into the pharmacy information system. Addresses insurance, reimbursement, and payment issues as approp

SHIFT Night (United States of America) Seeking Breakthrough Makers Children's Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation. At CHOP, your experience is valued; your voice is heard; and your contributions make

Site Name USA Pennsylvania Upper Providence, Durham Blackwell Street, GSK House, Rockville Biopharm, Stevenage, UK Hertfordshire Ware, Waltham, Zug House Posted Date Feb 22 2024 Are you looking for a role where you will serve as a key strategic partner representing Global Regulatory activities? If so, this Director of Regulatory Affairs, CMC could be an exciting opportuni

Responsibilities Essential Duties Follows established procedures and guidelines to manufacture the organization's products according to production specifications and schedules, volume, cost, and wastage targets or quality standards. Operates machines and production equipment safely and in accordance with instructions. Monitors the quality of output to identify, discard or

(Primary function) The Associate Director Director, PreClinical QA provides oversight of regulated laboratory activities and ensures that quality systems are developed and maintained to regulatory standards and Incyte standards. This position is responsible for leading, developing, and maintaining the quality assurance programs, audit functions and policies for Incyte Pre

This individual will require an understanding of the scope of Medical Affairs training and excellence as well as excellent organizational and project management skills. The position will deliver by building strong relationships with key partners in a highly matrixed team environment. This role is accountable for executing the US Medical Affairs (USMA) training objectives,

PHARMACY TECHNICIAN MID SHIFT Job Locations US PA BETHLEHEM ID 2024 143339 Line of Business PharMerica Position Type Full Time Our Company PharMerica Overview Join our PharMerica team! PharMerica is a closed door pharmacy where you can focus on fulfilling the pharmaceutical needs of our long term care and senior living clients. We offer a non retail pharmacy environment.