Medical Affairs Consultant

The Role The Sr. Scientist/Scientist, US Medical Affairs, will provide scientific/medical support for Genmab assets in various stages of development, involved in the execution and implementation of the Medical Affairs strategy.  She/he will provide scientific/medical and operational input into core medical affairs activities such as internal and external...

Role & Responsibilities Strong working in the Medical Affairs. Work with Med. Affairs team to create initial SOP creation and revision Websites Digital document storage and retention and Inspection Readiness preparation. Create review track and manage clear and concise medical information including Standard Response letters and fulfillment of ad hoc...

The Head of US Medical - Endocrine Medical Affairs will report to the US General Manager with primary responsibility to lead the US Medical Directors and ensure the compliant execution of all medical programs and functions associated with the late-stage development and medical aspects of commercialization of endocrine assets at Ascendis Pharma. In addition...

Role & Responsibilities Strong working in the Medical Affairs. Work with Med. Affairs team to create initial SOP creation and revision Websites Digital document storage and retention and Inspection Readiness preparation. Create review track and manage clear and concise medical information including Standard Response letters and fulfillment of ad...

PMV Pharmaceuticals Inc. Job Description: Executive Director, Head of Regulatory Affairs Reports to: Chief Development Officer Location: Hybrid (2 days a week in Princeton, NJ office)Position Overview The Executive Director, Head of Regulatory Affairs position will provide regulatory expertise and leadership to ensure that the company meets its objectives....

Job DescriptionJob DescriptionPMV Pharmaceuticals Inc.Job Description: Executive Director, Head of Regulatory AffairsReports to: Chief Development OfficerLocation: Hybrid (2 days a week in Princeton, NJ office)Position OverviewThe Executive Director, Head of Regulatory Affairs position will provide regulatory expertise and leadership to ensure that the...

Job DescriptionJob DescriptionOur Pharmaceutical client seeks a Global Director Regulatory Affairs Strategy to guide global teams through the development and execution of regulatory strategy and the design of CMC components of drug development programs in collaboration with counterparts, investigators, project team members, and consultants. Lead/support...

Our client is looking to fill the role of HEOR Consultant. This position will be fully remote. This position serves as the lead for HTA launch readiness projects for Nephrology products. Supports under the Director, Health Outcomes this individual will develop elements of a dossier, Systematic lit reviews and HE models, used to deliver on evidence strategy...

Job DescriptionJob DescriptionOur Pharmaceutical client seeks a Global Director Regulatory Affairs Strategy to guide global teams through the development and execution of regulatory strategy and the design of CMC components of drug development programs in collaboration with counterparts, investigators, project team members, and consultants. Lead/support...

Manager Global Regulatory AffairsPrinceton, New JerseyEU GMP requirementsMust have Global Regulatory Affairs experience in the pharmaceutical or biotechnology industry.Are you looking to make a career change to a stable company? This exciting opportunity offers a competitive salary plus an excellent benefits package including medical insurance, dental...

The HEOR Consultant/VRWE Scientist serves as the lead for individual projects in support for HTA launch readiness projects for Nephrology products. Under the strategic lead of a Director, Health Outcomes, and working with cross-functional teams, the VRWE Scientist develops elements of a dossier, HE models, and Systematic lit reviews which will be used in...

The HEOR Consultant/VRWE Scientist serves as the lead for individual projects in support for HTA launch readiness projects for Nephrology products. Under the strategic lead of a Director, Health Outcomes, and working with cross-functional teams, the VRWE Scientist develops elements of a dossier, HE models, and Systematic lit reviews which will be used in...

The HEOR Consultant/VRWE Scientist serves as the lead for individual projects in support for HTA launch readiness projects for Nephrology products. Under the strategic lead of a Director, Health Outcomes, and working with cross-functional teams, the VRWE Scientist develops elements of a dossier, HE models, and Systematic lit reviews which will be used in...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Job Title: Senior Managing Consultant - Quality, Regulatory & Compliance (Life Science) This unique opportunity acts as a gateway into a dynamic consulting function within the wider industry side business. As a Senior Managing Consultant, you will be a part of the end-to-end solution for a portfolio of pharmaceutical clients, spearheading innovative...

Role & responsibilities Strong working in the Medical Affairs Work with Med. Affairs team to create initial SOP creation and revision Websites Digital document storage and retention and Inspection Readiness preparation Create review track and manage clear and concise medical information including Standard Response letters and fulfillment of ad hoc...

Our Pharma client is currently searching for a Medical Science Liaison to effectively engage with healthcare partners and providers and to communicate strategic objectives. The Medical Science Liaison will educate and communicate value, outcomes and economic data to payers and providers and to help identify new opportunities. The Medical Sciences Liaison...

Role & responsibilities Strong working in the Medical Affairs Work with Med. Affairs team to create initial SOP creation and revision Websites Digital document storage and retention and Inspection Readiness preparation Create review track and manage clear and concise medical information including Standard Response letters and fulfillment of ad hoc requests...

We at **Medical Essential Diagnostics**, which is a rapidly growing healthcare provider for all frontline workers in the state of New Jersey. We take pride in our frontliners and want to give them as many opportunities as possible to be in their peak physical condition while they are serving our communities. We perform comprehensive and confidential testing...

Job DescriptionJob DescriptionAscendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology. Here at Ascendis, we pride ourselves on exceptional science, visionary leadership, and skilled and passionate...