The Associate Director of Clinical Pharmacology will have a key role in advancing our growing pipeline. The ideal candidate will champion the use of clinical pharmacology expertise and model informed drug development (MIDD) strategies to enhance the development of novel therapies across all phases of R&D and therapeutic areas, including neurology, ophthalmology, and rare

Drive translational research and development efforts by conducting experiments alongside R&D Scientists in the drug discovery department. Conduct a wide range of biochemistry, molecular and cellular biology techniques to express, purify and characterize drug candidates (e.g. DNA/RNA isolation, plasmid construction, PCR, Octet, HPLC, mammalian cell culture, transient and s

Currently hiring a Principal Clinical Regulatory Medical Writer to work r emote from any location in the US. ( Full time) The Principal Medical Writer will research, create, and edit all documents associated with clinical research. The Principal Medical Writer may operate as the project lead writer/submission coordinator and primary client contact to manage contributions

We are seeking a Research Technician to support the lab of Dr. Ben Tu at the UT Southwestern Medical Center in Dallas, Texas. The Tu Lab is investigating the relationship between cellular metabolism, nutrition, and fundamental regulatory processes. Working in mice, they are exploring novel and unexpected links between metabolism, cell growth, and disease in mammals. This

About Inari... Inari is the SEEDesign company. We embrace the diversity and complexity of nature in every aspect of our business to drive innovation to push the boundaries of what is possible. Through our unrivaled technology platform, Inari uses predictive design and advanced multiplex gene editing to develop step change products. We are taking a nature positive approach

DETAILS This position develops, documents and executes pre market and post market clinical evidence strategies for medical devices across product platforms. Works with cross functional teams and key stakeholders to execute on clinical evidence strategies for specific products/product families. For established products in the EU market, writes post market clinical follow up

of Role Perform routine and advanced testing on incoming materials, finished products and stability studies in QC Laboratory. Perform routine environmental monitoring and utilities testing. Area Specific Requirements Familiar with aseptic technique Perform Environmental Monitoring and utilities monitoring. Perform bioburden, sterility, endotoxin and other routine and advan

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

The Director of Global Medical Affairs Strategy, Ophthalmology is a key member of the global medical affairs team who will work closely with medical affairs and cross functional stakeholders to implement key aspects of the global medical affairs strategy for ophthalmology. The successful candidate will drive strategic execution across medical affairs activities, which may

Comprehends, manages, and executes the commercial Promotional Review Committee (PRC)/Medical, Legal, and Regulatory (MLR) review process, ensuring all tactical plans are implemented in compliance with the promotional guidelines and hold all stakeholders accountable by reinforcing the process Work with Marketing/Commercial to coordinate and prioritize materials for Promoti

The Associate Director, Ophthalmology is a key member of the Global Medical Affairs team who will work closely with medical affairs and cross functional stakeholders to implement key aspects of the Global Medical strategy for ophthalmology and potential global launches of pegcetacoplan in geographic atrophy (GA) secondary to age related macular degeneration (AMD). These a

The Field Reimbursement Manager (FRM) helps minimize access & reimbursement barriers for patients and providers to optimize access to Apellis' Ophthalmology portfolio. Within their geography, the FRM is responsible for addressing access barriers by strategically working with customers and accounts to solve the most complex patient access issues through all facets of the r

Reporting to the Anatomic Pathology Operations Manager, the histotechnologist accurately and proficiently prepares tissue slides according to established procedures in order to provide efficient, high quality products. Full rotation on immunohistochemistry and special stains. Assures total compliance with JC and CAP guidelines during all procedures and consistently observ

of Key Responsibilities Provides leadership and guidance to various stakeholders to ensure development and implementation of innovative global regulatory strategies across Alnylam's portfolio of combination/device products Provides technical, strategic and tactical regulatory guidance to matrixed product development teams Defines and optimizes global regulatory strategies

In order of importance, list essential areas of responsibility, major job duties, special projects and key objectives for this position. These items should be evaluated throughout the year and included in the written annual evaluation. This section should be completed as a bulleted list and explain how the role is performed. Maintains electronic laboratory notebook Unders