Associate Director, Senior Study Lead – Single Sponsor Dedicated

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🇬🇧 United Kingdom – Remote

⏰ Full Time

🟠 Senior

👔 Director

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

⚕️ Healthcare Insurance

🧬 Biotechnology

🤖 Artificial Intelligence

💰 $1G Post-IPO Debt on 2023-05

Healthcare Insurance • Biotechnology • Artificial Intelligence

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to 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.

🎯 Requirements

• 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.

🏖️ Benefits

• Flexible working arrangements