Associate Director, Senior Study Lead – Single Sponsor Dedicated

🕒 il y a 1 mois

🇬🇧 Royaume-Uni – Télétravail

⏰ Temps Plein

🟠 Senior

👔 Directeur

🇬🇧 Parrain de Visa de Travailleur Qualifié UK

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

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IQVIA

Site WebLinkedInTous les Emplois

10 000+ employés

💼 Conseil

🏭 Fabrication

📣 Marketing

💰 €1 000 000 000 Post-IPO Debt en 2023-05

Consulting • Manufacturing • Marketing

IQVIA est un leader mondial dans le domaine de l'analyse de données et des solutions technologiques, dédié à l'amélioration des résultats de santé. L'entreprise utilise sa plateforme Connected Intelligence pour exploiter la puissance des analyses de données avancées et de l'intelligence artificielle, favorisant ainsi l'innovation dans le secteur de la santé. IQVIA se concentre sur divers domaines, y compris la recherche clinique, la technologie et les services de conseil, afin de résoudre des défis complexes dans le domaine de la santé et d'accélérer la livraison de nouvelles thérapies aux patients.

Description

• The Associate Director Senior Study Lead is the leader of the cross-functional clinical trial team (CTT), who guides planning and management of the assigned clinical study/studies end-to-end to achieve objectives. • Accountable for proactive, iterative operational planning with effective contingencies and embedded risk management mindset in CTT. • Oversees budget and people allocation within assigned study/studies. • Contributes in promoting operational excellence through process improvement and knowledge sharing across studies. • Fosters an empowered, psychologically safe organization that can navigate a matrix environment, learns, and adjusts quickly to changing conditions and business needs.

🎯 Exigences

• Bachelor's degree in life sciences/healthcare (or clinically relevant degree) is required. • Advanced degree is strongly preferred. • ≥ 4 years of recent involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV of standard to high complexity and priority. • ≥ 3 years of recent contribution to and accomplishment in all aspects of conducting clinical studies of standard to high complexity and priority (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry or a contract research organization, including expert knowledge of international standards (GCP/ICH), health authorities (FDA/EMA), local/National Health Authorities • Experience in managing people globally in a complex matrix environment preferred • Management of virtual teams. • Proven ability and strong experience leading teams and building capabilities • Experience in developing effective working relationships with internal and external stakeholders • Excellent communicator and presenter (oral and written); ability to communicate at all levels • Excellent organization and prioritization • Strong negotiation and conflict resolution skills and enterprise mindset, demonstrated by ability to drive for aligned solutions • Fluent English, oral and written.

🏖️ Avantages

• Flexible working arrangements