Associate Director, Clinical Operations

🕒 il y a 1 mois

🇬🇧 Royaume-Uni – Télétravail

⏰ Temps Plein

🟠 Senior

🏥 Responsable des Opérations Cliniques

🇬🇧 Parrain de Visa de Travailleur Qualifié UK

Cette entreprise a parrainé des visas de Travailleur Qualifié du Royaume-Uni par le passé.

👻 Score fantôme 29%

Ce que ça veut dire : la probabilité que cette offre reste ouverte sans recrutement actif.Comment le lire : 60 % ou plus, on pense que c'est une offre fantôme. Un score plus bas est moins inquiétant.Comment on la calcule : ancienneté, republications, postes ouverts vs taille de l'équipe, rapidité de clôture, et si le salaire est indiqué.À noter : une estimation à partir de données publiques, pas un jugement sur l'entreprise. De vraies offres peuvent avoir un score élevé, alors prenez-le comme un indice, pas comme un fait.

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Jazz Pharmaceuticals

Site WebLinkedInTous les Emplois

1001 - 5000 employés

Fondée en 2003

🏥 Santé

🏭 Fabrication

🧬 Biotechnologie

Healthcare • Manufacturing • Biotechnology

Jazz Pharmaceuticals est une entreprise biopharmaceutique dédiée au développement de médicaments innovants répondant à des besoins médicaux sérieux non satisfaits. Avec un fort engagement envers la recherche et le développement, Jazz se concentre sur la création de thérapies transformatrices, mettant en avant l'importance de la collaboration, de la diversité et de l'engagement des employés dans ses opérations. L'entreprise est fière de transformer la vie des patients grâce à ses offres de produits significatives et une culture qui favorise l'enthousiasme et la flexibilité.

Description

• Provide subject matter expertise and contribute to the planning and delivery of a clinical development program to scope, quality, budget, time and managing risk as assigned by therapeutic and compound leadership • Partner with therapeutic and functional leadership to define and operationalize program strategy • Advise functional leadership on resourcing requirement for the applied operational strategy • Responsible for providing clinical operations expertise into the clinical development plans for review by governance committees • Drive the development and alignment of clinical documents (protocols, clinical study reports, investigator brochures, etc.), providing clinical operations expertise. • Provide clinical operations expertise into the country selection and feasibility to support project start-up and delivery • Oversee study team deliverables, including enrollment, milestones, and inspection readiness • Develop and oversee program timelines, budgets, forecasts, and key deliverables to ensure programs are executed on time, within budget, and with quality • Contribute to study scope and provide approvals within delegated authority; contribute to vendor selection, contracting, and ongoing oversight to ensure quality, compliance, and performance • Identify risks and issues related to program deliverables; develop and implement mitigation and action plans • Act as the point of escalation for clinical study teams for risk and issues related to clinical studies, sites, and vendors • Drive operational excellence across clinical programs through cross-functional collaboration with Clinical Development, Data Management, Biostatistics, Regulatory, and other stakeholders • Responsible for leadership and program management of non-drug project work as assigned, e.g. cross functional improvement/change initiatives • Contribute to functional and cross-functional initiatives as Subject Matter Experts • Mentor, coach and support people development as appropriate • Actively participate in networking both within and outside the therapeutic area, sharing best practices and lesson learnt • Be an early adopter for new ways of working and act as an ambassador for change, driving the implementation and utilization of initiative outputs.

🎯 Exigences

• Extensive experience in clinical research within the pharmaceutical or biotechnology industry (typically 10+ years) • Proficient understanding of global clinical trial regulations, ICH/GCP guidelines, and regulatory compliance requirements • Capability to interact with functional leaders and major vendors, and in some cases senior leadership, on matters concerning program strategy and execution • Proficient financial acumen in managing clinical trial budgets, forecasting spend, and making cost-effective operational decisions aligned with program goals • Proven ability to collaborate cross-functionally and influence stakeholders to drive strategic and operational decisions • Leadership capabilities, including the ability to mentor, influence, and drive team or matrix performance • Ability to manage complex projects, prioritize competing demands, and solve problems in a fast-paced environment • Bachelor of Science/Master of Science degree in a related discipline, or equivalent work experience. Advanced degree is preferred.

🏖️ Avantages

• medical, dental and vision insurance • retirement savings plan • flexible paid vacation