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Associate Director, Transnational MedicineRef: BBBH23641

Salary:€130000 - €145000 per annum + 12% bonus

Added:08 Nov 2018

Region: Europe

Sector: Pharmaceutical

Sub Sector: Clinical Research

The Associate Director, Translational Medicine will: *Lead multidisciplinary and cross-organizational project teams *Be responsible for establishing and agreeing a viable project drug development strategy to satisfy Target Product Profile requirements *Provide scientific leadership on different aspects of the project and align relevant team members and experts *Be responsible for preparing data-driven recommendations for management decisions and to the Joint Steering Committee for partnered projects *Take active part in advisory boards, meetings with scientific committees, and regulators *Proactively manage collaborations with partners and represent the client - aligned strategy and implementation *Engage with the selection and management of external vendors for conducting preclinical and clinical activities *Develop and maintain an approved project plan and associated budget *Be accountable for delivering on project plan according to timelines, budget, operational procedures, Quality standards, and for reporting progress to donors *Be responsible for successfully transitioning projects to the late-stage development project leader *Ensure accuracy of all internal and external communications relating to the project Education and Experience: *PhD in life sciences *Minimum 8-10 years of drug development experience at a pharmaceutical or biotech company *Must have >5 years of experience in leading complex projects in preclinical/early stage development (phase I and II), in collaboration with external companies would be a plus *Demonstrated success in positions involving influencing and negotiation *Experience in anti-infective therapeutic area, drug combination development and pediatric therapeutics is desired Technical skills required: *Proven ability to successfully lead multiple projects in a drug development environment *Scientific expertise in preclinical/early stage drug development with emphasis on clinical aspects *Broad working knowledge of non-clinical, formulation development, Chemistry, Manufacturing & Controls (CMC) and other aspects of drug development *Experience in working with late-stage development and market access groups to align drug development strategy with target product profiles *Knowledge of ICH / GLP & GCP guidelines *Fluency in English (oral and written) *Familiar with common computer statistical, technical, and database applications Key People is a specialist international recruitment consultancy with over 25 years' experience of working within the life sciences, biotech, healthcare and CRO industries. Our experienced and dedicated clinical research related consultants have a long history of success, excellent technical knowledge and a flexible, consultative focussed approach to recruitment. Please contact Mark Cussens, Clinical Research Recruiter on Tel: +44 1727 817623 or email: mcussens@keypeople.co.uk Tel: +41 4350 86620 or email: mark.cussens@keypeopleswitzerland.ch Key People is a recruitment company with a reputation for providing good value that's been built up over 20 years. -We achieve results faster -Our candidates really are a cut above -We add greater value For our candidates, we have developed relationships with thousands of clients nationwide and across Europe, who choose to recruit through Key People, so you'll have a wide choice of opportunities to further your career.

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