of Role Responsible for integrating and applying advanced knowledge of global regulations governing pharmaceutical drug development and commercialization to all aspects of assigned preclinical and/or clinical drug development programs, policies, and procedures, to ensure the rapid and successful development and registration of products while maintaining compliance with all

Develop, implement, and lead the regulatory regional strategy, in alignment with company goals, for new and sustaining ZOLL Resuscitation products and features. Essential Functions Develop and successfully implement regional regulatory strategies for new and sustaining products/features that result in device approval. Ensure project team colleagues, line management, and k

Co lead the strategy and implementation of global regulatory strategies for In Vitro Diagnostics (IVD)/Companion Diagnostics (CDx) to support business objectives. Act as the interface with multiple internal and external stakeholders, including partners. Works as Global Regulatory Leads (GRLs) for assigned projects. Positively contributes to the regulatory probability of su

The Senior Director, Scientific Communications is a seasoned Medical Affairs professional with an established track record of creating, leading, and delivering high impact scientific publication and communication program(s). S/he will oversee publication planning and execution along with being an integral part of Program Team(s) across the Keros portfolio. Areas of focus

of Role Plans, organizes, directs and reports on quality activities to assure external partners and suppliers meet or exceed Lantheus' requirements for Pharmaceutical Products and Positron Emission Tomography (PET) Drug manufacturing. Key Responsibilities/Essential Functions Works closely with cross functional teams, including senior management levels, to ensure Lantheus m

Are you a current UMass Memorial Health caregiver? CLICK HERE to apply through your Workday account. Schedule Details Monday through Friday, Weekends (Saturday and Sunday) Scheduled Hours 630am to 715p Shift 4 Mixed Shift, 8 Hours (United States of America) Hours 0 This position may have a signing bonus available a member of the Recruitment Team will confirm eligibility d

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

Are you ready to join a team committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines? At Kura Oncology, you have an opportunity to be a part of something bigger, with a lasting impact that you can be proud of. At Kura Oncology, we are working to change the paradigm and improve the science of cancer treatment

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

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

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

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

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

Post Doc (0) Minimum Salary US MA Worcester Job Location 17 hours ago (5/2/2024 12 28 PM) Requisition Number 2024 45870 # of Openings 1 Posted Date Day Shift Exempt Exempt/Non Exempt Status Non Union Position W63 Residents/Post Docs Overview The Department of Biochemistry and Molecular Biotechnology and the Program in Chemical Biology jointly invite applications for a pos