Are you passionate about revolutionizing healthcare through innovative medical devices and cutting-edge AI technology? We are seeking a dynamic and experienced Director of Regulatory Affairs to join our team in the vibrant San Francisco Bay Area. As the Director of Regulatory Affairs, you will play ...
Works collaboratively with Medical Scientists, Medical Information, Clinical Research, and Clinical Pharmacology and Commercial to support responses to medical inquiries and slide development. Works collaboratively with Medical Scientists, Medical Information, Clinical Research, and Clinical Pharmac...
Serving as a value-added resource and extension of The Company’s US Medical Affairs organization, the Medical Science Liaison (MSL) will support the Company’s Global Medical Affairs team. The MSL will serve as a liaison between The Company’s Medical Affairs and the clinical study sites, investigator...
S/he will work cross-functionally with other leaders and functions (including all Medical Affairs functions, Commercial, Compliance, IT, Finance, Clinical Development and Legal) to drive from inception to completion all Rare Disease MA workstreams and projects and to provide relevant medical input o...
This position is located in the Laboratory and Pathology Service at VA San Diego Health Care System - Jennifer Moreno VA Medical Center in San Diego, CA. The Medical Technician performs specimen collection, processing, accessioning and waived testing in one of the facilities within VISN 22. Particip...
Executive Director (ED) Global Medical Affairs (GMA) Liver Diseases and HIV Prevention- Remote Responsibilities:The ED GMA-Liver Diseases and HIV Prevention is a key position serving the Global Medical Affairs. Liver, Inflammation, Fibrosis and Est Director, Medical, Clinical Research, Executive, G...
Medical Director will lead the development and execution of the medical strategy for Rett Syndrome. Primary Responsibilities</u></strong></p><ul><li>Provide scientific and medical leadership, including development of strategic plans, identifying specific unmet medical n...
As an Executive in this area, they have 5 priorities: the execution of Halozyme sponsored clinical trials, development and execution of the Medical Affairs plan to support Halozyme commercial products, medical leadership of input into ENHANZE partner development programs including support of regulat...
S/he will work cross-functionally with other leaders and functions (including all Medical Affairs functions, Commercial, Compliance, IT, Finance, Clinical Development and Legal) to drive from inception to completion all Rare Disease MA workstreams and projects and to provide relevant medical input o...
Executive Director (ED) Global Medical Affairs (GMA) – Liver Diseases and HIV Prevention- Remote. The ED GMA-Liver Diseases and HIV Prevention is a key position serving the Global Medical Affairs. An integral part of the Liver and HIV Prevention Global Medical Affairs strategy will be overseeing and...
The Medical Director (Medical Affairs) will report into the Medical Affairs Department and is responsible for clinical support and consultative activities across the PBM. The Medical Director (Medical Affairs) will report into the Medical Affairs Department and is responsible for clinical support an...
Executive Director (ED) Global Medical Affairs (GMA) – Liver Diseases and HIV Prevention- Remote. The ED GMA-Liver Diseases and HIV Prevention is a key position serving the Global Medical Affairs. An integral part of the Liver and HIV Prevention Global Medical Affairs strategy will be overseeing and...
Education and/or Experience: (1) A bachelor's degree or higher from an accredited college or university in medical laboratory science, medical technology, clinical laboratory science or in a related science (, laboratory sciences such as chemistry, biochemistry, biology, microbiology, immunology, et...
Engage in meaningful, peer-to-peer scientific exchange of medical and scientific information with the oncology and hematology community, consistent with the integrated Medical Affairs Plan (iMAP). Support medical/scientific training of cross functional teams and contribute in external medical educat...
This position will be reporting into the SVP of Regulatory Affairs and will be supporting Clinical Regulatory and Regulatory CMC functions. Senior Director, Regulatory Affairs (Generalist). Meet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affair...
Manager, Regulatory will work closely with cross-functional teams to help determine regulatory strategies and ensure compliance with all applicable regulations. VP, QC/Regulatory and help provide leadership and management direction for all regulatory compliance activities on a domestic and internati...
Activities include conducting scientific presentations to health care providers, in particular pulmonologists, emphasizing the medical and scientific strengths and differences of company's diagnostic tests as well as with any future company development initiatives. The position requires a profession...
A rapidly growing EPC company are looking for a Solar Project Manager. You will have the opportunity to lead a team of Project Managers as you progress through the company. Leading the project plan, ensuring successful project execution throughout all stages, from sales and engineering to constructi...
The Regulatory Affairs Specialist IV will coordinate the accumulation of technical information and prepare submissions for in vitro diagnostic and medical device licenses to various governmental regulatory agencies. Drafts, edits and compiles technical documentation and design dossier in support of ...
Director CMC Regulatory Affairs. They are currently seeking a skilled regulatory professional to join their growing team as Director/ Sr. Offering regulatory advice to cross-functional teams, leading the drafting of submission responses to regulatory queries, and collaborating with CMC and Quality d...
Manager of Regulatory Affairs to play a part in their early and late stage clinical trials. Provide leadership to the regulatory therapy area team. Manage regulatory interface with domestic and international health authorities. Develop and deploy regulatory programs for product approval. ...
Lead teams in evaluating strategy options, identifying and mitigating regulatory risks, and guiding successful regulatory interactions. Bachelor’s degree in life sciences; 10+ years of biopharmaceutical Regulatory Affairs experience. Provide regulatory guidance to project teams, collaborating with c...
As a Regulatory Affairs Specialist, you will be a key player in our R&D team, ensuring our Quest and Atkins brands comply with all domestic and international laws and regulations. Are you a detail-oriented professional with a passion for regulatory compliance? Do you excel in ensuring products meet ...
We are seeking a PT Construction Project Manager, to join our dynamic team. As a Construction Project Manager at HOHM, you will be working closely with our partner Build Teams, customers and reporting directly to top level management. ...