20 set - Bardi
Iqvia
Overview
In this role you lead strategic delivery of global clinical trials, partnering with sponsors and cross-functional teams to accelerate development of innovative therapies.
You guide multi-regional studies, ensuring quality, timelines and budget alignment while navigating regulatory requirements.
You work with senior sponsors to provide strategic solutions and shape study outcomes.
This role offers broad global exposure, leadership impact, and the chance to advance patient outcomes through cutting-edge research.
Responsabilità
Lead delivery of complex global and multi-regional clinical studies, ensuring operational excellence
Act as primary strategic partner for sponsors, offering leadership and innovative solutions
Provide direction to cross-functional regional teams to drive collaboration and accountability
Oversee study timelines, budgets, quality, risks, and financial performance
Drive proactive risk management, issue resolution, and stakeholder alignment
Ensure studies comply with ICH-GCP,
regulatory requirements, and contractual commitments
Requisiti fondamentali
Bachelor's degree in Life Sciences or related discipline
7+ years of clinical research experience with global or multi-regional trials in CRO/pharma/biotech
Experience leading renal, obesity and/or MASH global studies preferred
Strong knowledge of clinical trial conduct, ICH-GCP, and regulatory requirements
Proven success in leading cross-functional teams and managing study delivery (timelines, budgets, quality, risks)
Ability to build trusted sponsor relationships and manage senior stakeholders
Excellent leadership, communication, problem-solving, and decision-making skills
Passion for advancing clinical research and patient outcomes
leadership
communication
problem-solving
ICH-GCP compliance
regulatory knowledge
study delivery management
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