MEDICAL DIRECTOR REGULATORY STRATEGY jobs in CAMBRIDGE, United Kingdom

Title: Senior Director, US Commercial Regulatory Affairs Company: Ipsen Biopharmaceuticals Inc.... Finally, this role works with cross-functional areas to determine the appropriate strategy for labels for regulatory authority...

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...

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

Director of Regulatory Affairs will be responsible for the development and execution of regulatory strategy for assigned... BicycleTx programs or projects. The Associate Director Regulatory Affairs will be responsible for oversight of the operational...

. Job Description As a Director, Global Regulatory Affairs, Precision Medicine you will develop and execute Precision Medicine regulatory strategies... in alignment with the drug global regulatory strategy in collaboration with cross functional stakeholders across the...

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

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...

will include defining the regulatory strategy, plans, and objectives for assigned products or projects. Additionally.... Job Description We are looking for an experienced Regulatory professional to join our global team. Location: Cambridge or Uxbridge. In this role...

agencies. You will lead and oversee the Global Regulatory Affairs (GRA) Labeling organization, inclusive of labeling strategy... experience and significant successes setting and directing the regulatory labeling or related strategy to successful conclusion...

and closely interact with the medical director(s) as well as with the biostatistics, regulatory, translational, and discovery... Director) to provide scientific support for all clinical development activities involving the conduct of clinical studies...

Title: Associate Director, Marketing, Rare Disease Company: Ipsen Biopharmaceuticals Inc... compliant development of field resources in line with the strategy Cross functional team lead-stakeholder management...

support for all project related activities for multiple products. Provides medical strategy and input into key regulatory... in therapeutic areas Defines global product safety strategy and routinely manages and leads functional and cross...

. Job Description POSITION OVERVIEW: Develops or oversees and ensures that strategic scientific and regulatory input relative to safety... with regulatory requirements and Gilead business practices. Demonstrates project management skills and knowledge of project...

There aren’t many Programme Managers like you. Because very few have worked on Active Implantable Medical Device...’s, tinnitus, and chronic pain. The global innovation race within neurotechnology presents exciting new opportunities for medical...

with Medical Dev. Director (MDD) and other relevant Ipsen team members Lead clinical project processes Lead cross-functional... conjunction with Clinical Development Program Directors (CDPDs), Medical Dev. Directors (MDDs), and other Ipsen team members...

. In collaboration with the director drug safety work to ensure compliance with GVP, GCP and global regulatory requirements... development of safety standards and processes. Main Responsibilities: In collaboration with the Director of Drug Safety...

collaboration with the Director of Drug Safety, participate in monitoring, review, analyses, interpretation and evaluation... safety signals. Contribute to the strategy and review of safety assessments and for signals or issues (including product...