/JOB PURPOSE Responsible for managing and maintaining existing investigational new drug (IND) and clinical trial application (CTA) submissions and preparing amendments in compliance with guidelines and regulations. Coordinates, compiles, and tracks product applications to regulatory agencies. Essential Duties And Responsibilities Review clinical site regulatory documents t

Site Name UK Hertfordshire Stevenage, Cambridge MA, USA Massachusetts Waltham, USA North Carolina Durham, USA Pennsylvania Upper Providence Posted Date Mar 4 2024 Associate Director/Director, Quantitative Systems Pharmacology The Department of Clinical Pharmacology Modelling and Simulation (CPMS) at GSK is recruiting for an Associate Director/or Director level Quantitativ

SHIFT Day (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 a

providing superior service and care. Position Specific Benefits include We offer a number of employee discounts to various activities, services and vendors... And parking is always free! Position Nuclear Medicine Technologist Shift Per Diem, flexible availability Experience Minimum 1 year of recent Nuclear Medicine experience preferred Education Graduate of an approved pr

Company Description Today is a new day. At Asbury we're filling it with more laughter, more possibilities, more ways to give back, all backed by support for whatever life brings your way. We are an organization with a mindset to help others, a place where seniors continue to teach, learn, and grow, a certified Great Place to Work where you can build a purposeful career. Le

PHARMACIST CONSULTANT Job Locations US PA BETHLEHEM | US PA HARRISBURG | US PA WILKES BARRE | US PA PHILADELPHIA ID 2024 143005 Line of Business PharMerica Position Type Full Time Our Company PharMerica Overview Our Pharmacy group focuses on providing exceptional customer service and meeting the pharmacy needs for hospitals, rehabilitation hospitals, long term acute care

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,

Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Responsibilities Essential Duties Adheres to all CAPS policies and procedures Prepares compounded sterile products using aseptic technique. Assists in the setup of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using ase

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Participates on project teams to advance discovery portfolio projects. Presents/defends scientific findings in multi functional project teams/initiatives Independently designs, analyzes, and interprets experimental results and technical reports, etc. Support Molecular Biology experiments for designing expression vectors. Protein expression experience in Mammalian and E.co

(Primary function) As a member of the US Marketing / Product Strategy team, the candidate for this position will play a pivotal role in the development and execution of the marketing programs to support the launch of a new product in GVHD.. The candidate will help lead the development and execution of marketing initiatives focused on health care professionals and patients.

Customer Retention Maximize customer retention rates by ensuring customer satisfaction, executing pre defined customer touch point/call plan, leading customer training (on site, as needed), anticipating and defending against competitive threats, and leveraging strategic selling framework Menu Expansion Proactively team with CEM & HSE to identify and close menu expansion o

The Manager of Global Medical Affairs, Independent Medical Education (IME) Grants will be responsible for the successful development and management of the global medical education grant program for assigned therapeutic areas (Tas). The position will support delivery of impactful medical education that enhances patient care by improving Healthcare Professionals' ability to

Senior Regulatory Affairs Associate Experience Biologic CMC 5+ years of experience Supported the CMC activities related to Vaccine/Biologic manufacturing and control including authoring of submission dossiers related to new application, post approval variations Understanding of EU/CA/WHO/US regulations & guidance allowing appropriate review and compilation of data to appr

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