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 Scientist I, Chemistry contributes to PTC's drug discovery efforts by synthesizing small molecules in support of internal lead optimization programs. The incumbent is responsible for independently planning and executing synthetic organic chemistry protocols to efficiently obtain desired targets for biological assays. The selected candidate is also responsible for inte

Contribute to project related molecular/microbiology tasks by strain construction using modern molecular biology and molecular genetics. Support optimization, analysis, and improvement of cell factories based on omics data analysis using molecular editing tools. Identify, investigate, and implement new and emerging technologies in relevant fields. Work with a multidiscipl

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

The Thought Leader Liaison (TLL) is responsible for developing, managing, and engaging with Key Opinion Leaders throughout their assigned geography reporting to the Thought Leader Liaison Lead, reporting through Specialty Brands Marketing. He/she works closely with commercial colleagues and other staff to help build advocacy of Mallinckrodt's products with KOLs. TheThough

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

Under supervision, performs laboratory analyses of raw materials, in process (IP), finished products (FP) and stability (ST) samples for pilot and submission batches, according to SOPs and cGMP procedures. Prepares method validation protocols/reports, and carries out method validation activities, including interim method validation, to meet project timelines. Supports lab

PHARMACIST CONSULTANT Job Locations US PA HORSHAM | US PA BETHLEHEM | US PA HARRISBURG ID 2024 142024 Line of Business PharMerica Position Type Full Time Pay Min USD $57.00/Hr. Pay Max USD $59.00/Hr. Our Company PharMerica Overview Our Pharmacy group focuses on providing exceptional customer service and meeting the pharmacy needs for hospitals, rehabilitation hospitals, l

(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

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,

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

The Assistant Director of Content Strategy for the Fox School of Business is responsible for developing content designed to enhance the overall reputation of the school, to communicate the Fox/STHM story to various stakeholders. The Assistant Director will primarily focus on publication efforts for the Fox Focus (Alumni magazine), On the Verge (Research magazine), and Con

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

Site Name UK Hertfordshire Ware RD, Durham Blackwell Street, GSK House, USA Pennsylvania Upper Providence Posted Date May 2 2024 As Regulatory Manager for devices, you will manage the overall global regulatory and advocacy strategy for GSK's portfolio of combination product devices (injectable and inhalation) across modalities and lifecycle We create a place where people

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