The Scientific Director provides high-level scientific and strategic leadership across global clinical development activities. This position plays a pivotal role in shaping long-term portfolio strategy, guiding evidence generation, and influencing key development decisions across early- and late-stage programs.You will lead cross-functional scientific teams, collaborate with international stakeholders, and ensure strong governance and oversight of external partners, contributing directly to the development of life-saving therapies.Key ResponsibilitiesStrategic & Scientific LeadershipContribute to global clinical development strategy and long-term portfolio planningProvide scientific guidance across early- and late-phase developmentLead study concept discussions and support regulatory-relevant documentationRepresent the organisation in scientific forums, governance committees, and external engagementsClinical DevelopmentSupport the design and refinement of clinical study plansEnsure scientific integrity, feasibility, and proactive issue resolutionContribute to timeline, resource, and budget planning for clinical programsCross-Functional LeadershipProvide scientific leadership across globally distributed teamsDrive alignment between Clinical Development, Regulatory Affairs, Medical Affairs, Biometrics, and related functionsStrengthen scientific capabilities, refine processes, and support organisational development initiativesLead evaluation and oversight of CROs and external scientific partnersEnsure high-quality deliverables aligned with programme and regulatory expectationsScientific Documentation & CommunicationLead authorship and review of key clinical and regulatory documents (CSR, CTD modules, development reports, expert statements)Contribute to regulatory submissions, advisory boards, scientific conferences, and senior-level interactionsRequirementsAdvanced degree (MD, Pharmacy, Life Sciences or related field); PhD or medical specialisation preferredExtensive experience in global clinical development strategy (early and late phase)Proven track record leading international clinical programmes and influencing portfolio strategyStrong knowledge of ICH, GCP, EMA, FDA frameworksHands-on regulatory submission experience (IND, IMPD, CTD modules)Demonstrated expertise in study design, evidence generation, target product profile development, and benefit–risk assessmentExperience managing departmental budgets and resource allocationFluent English (additional languages advantageous)
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