GLOBAL REGULATORY AND OPERATIONS jobs in CAMBRIDGE CB4, United Kingdom

Title: Director, Global Regulatory Affairs, Oncology Company: Ipsen Bioscience, Inc. Job Description: Director..., Global Regulatory Affairs, Oncology Summary / purpose of the position To be accountable for the strategy, tactics...

Affairs, Regulatory Affairs, Global Patient Safety, Clinical Operations, BioStats & Data Management, Clinical Quality...The Business Analysis & Operations Senior Manager will drive consistency across the Global Development (GD) IT team...

with Commercial Marketing, Medical Affairs, PRC/MRC Coordinators, Legal Affairs, Regulatory Affairs Strategy, Labeling Operations...Title: Associate Director, US Regulatory, Advertising & Promotion Company: Ipsen Biopharmaceuticals Inc...

of Prescription Drug Promotion (OPDP) as required, working with Global Regulatory Labeling to review and assess forth coming changes... and efficient promotional review process. Partner with Global Regulatory Strategy and Labeling on future/planned labeling updates...

's Global Regulatory Affairs organization and acts as a critical strategic partner across cross-functional teams. Regulatory... agencies. You will lead and oversee the Global Regulatory Affairs (GRA) Labeling organization, inclusive of labeling strategy...

filing plan (MA and Lifecycle maintenance). Collaborate with Regional and Global Study Operations (GSO) teams to support...CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Cambridge...

filing plan (MA and Lifecycle maintenance). Collaborate with Regional and Global Study Operations (GSO) teams to support...CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Cambridge...

. To provide regulatory expertise to R&D, Franchise and Commercial Operations for assigned products/projects. Act as the interface... between the R&D/Franchise/Operations and GRA on all regulatory issues relevant to Development and Product Maintenance activities...

. You will be responsible for the development of a CMC and device regulatory strategy, working closely with Technical Operations colleagues. The...: Responsible for the development and execution of global regulatory CMC and device strategies and submissions, including CMC...

Clinical Study Team activities for assigned clinical studies. The Global CPM, in concert with the Director Clinical Operations...Job Purpose As a Global Clinical Project Manager you are responsible for the management of all aspects of the...

Title: Associate Director, Global R&D and Medical Finance Company: Ipsen Bioscience, Inc.... Job Description: Associate Director, Global R&D and Medical Finance Summary/purpose of the position Associate Director, R&D Controller...

, with demonstrable experience in a GLP/GCP quality/compliance role Knowledge of GLP/GCLP and GCP global regulatory requirements... with high unmet medical need. Bicycle is headquartered in Cambridge, UK, and our US operations run out of Lexington...

operations are performed seamlessly, securely, and in compliance with Service Level Agreements (SLAs) and regulatory requirements... 5.5m customers every day in over 175 countries, with a global ecosystem of market-leading partners. Global strategic hubs: Spain...

We are Eversheds Sutherland, a global law firm, with 5,000+ colleagues in more than 30 countries. We're full service... As a lawyer, you enjoy a variety of work: regional to international and across practice groups. With us, you grow your global...

change in respiratory care through global deployment of its technologies, including in resource-poor countries. TidalSense..., including clinical, marketing, finance, and operations, to ensure alignment and execution of commercial objectives...

reports (in partnership with the product physician). Authors the SERM safety contribution to global regulatory submissions in... and benefit-risk management of the assigned portfolio of GSK global assets to ensure Patient Safety globally. If appointed...

with regulatory requirements, Good Clinical Practice (GCP) guidelines and SOPs to the most rigorous standards of quality, timely... the CPM in site selection, verify timely collection of essential study documents, such as regulatory and ethics committee...