Director, Clinical Science, Aesthetics

Posted 13 days 18 hours ago by Ipsen Group

£100,000 - £125,000 Annual
Permanent
Full Time
Other
London, United Kingdom
Job Description
Cookie Notice WHAT - Summary & Purpose of the Position WHAT - Main Responsibilities & Technical Competencies Leads and/or participates in marketing and clinical/medical advisory panels, steering committees and investigator meetings. Remains up to date with current information on pharmaceutical regulations, guidelines, and practices and therapeutic area knowledge and ensures consistent best practice across all activities. Provides expert scientific clinical development advice leadership to the project teams for the development of Phase I-IV clinical programs. Leads development of clinical studies and reviews clinical protocols, related documents, and clinical study reports for scientific and operational accuracy. Participates in drug safety surveillance for Development projects. Develop and demonstrate expertise in data review and interpretation to deliver meaningful efficacy and safety conclusions. Demonstrate the ability to interpret conclusions in context of product profiles and medical practice to create key messages, in collaboration with key stakeholders. Expertise in aesthetic drug development highly desired, but not required Demonstrated in-depth understanding of drug development and pharmaceutical marketing within therapy area. Working knowledge of regulations relating to drug development and promotional activities Demonstrated ability to communicate and plan effectively with other Ipsen departments and to respond to inquiries or complaints from customers. Demonstrated ability to effectively present information to senior management, employees at all levels of the organization, and external audiences. 5+ years experience of clinical research and organizational management within the pharmaceutical industry, a CRO, or similar organization. Demonstrated ability to collaborate in a matrixed environment Experience in submissions of IND/CTX/NDA/MAA and interactions with Regulatory authorities, and /or Experience in designing and conducting Phase I-III clinical trials; and/or significant late-stage development research Get In TouchIntroduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match.