ppThe bTrial Delivery Leader (TDL) /b serves as the bsingle point of accountability /b for btrial operational strategy, trial-level budget, quality, and on-time delivery /b of assigned clinical trials.
This role represents the bevolution of the Global Trial Leader (GTL) /b , with a stronger emphasis on strategic leadership, end-to-end accountability, and governance-level decision making.
/p pThe TDL works in close partnership with the bProgram Delivery Leader (PDL) /b and co-leads the bCross-Functional Trial Team (CFTT) /b to ensure trial strategies are aligned with program objectives and executed efficiently.
/p pThe Trial Delivery Leader plays a bcritical role in ensuring clinical trials are delivered efficiently, compliantly, and with high quality /b , while balancing speed, cost, and innovation.
By serving as the single point of accountability, the TDL enables clearer decision making, stronger execution, and improved trial outcomes across the development portfolio /p h3Scope of Focus /h3 pThe Trial Delivery Leader is primarily focused on bstrategic leadership and execution oversight /b , rather than administrative task execution.
Key focus areas include: /p ullipCo-leading the CFTT and driving cross-functional alignment /p /lilipCoordinating functional strategies (e.g., trial endpoints, ARBM, biomarkers, DEICT, digital health, companion diagnostics) /p /lilipEnsuring timely delivery of btrial-level deliverables /b /p /lilipTrial-level bbudget ownership and oversight /b /p /lilipQuality oversight and inspection readiness /p /lilipEarly operational input during binitial protocol development /b /p /lilipDevelopment of bcost-optimized and accelerated scenarios /b and innovative approaches, aligned with trial tiering (post-POC) /p /li /ul h3Key Accountabilities /h3 ullipDevelop the btrial operational strategy /b , integrating and aligning all btrial-level functional strategies /b into a single, holistic approach, including vendor strategy.
/p /lilipPartner closely with the bPDL /b to shape trial-level strategy in alignment with overall program strategy.
/p /lilipCo-lead the bCross-Functional Trial Team (CFTT) /b , setting meeting cadence, agendas, and expectations.
/p /lilipEmpower CFTT members to independently drive their functional deliverables while maintaining accountability for timelines and quality.
/p /lilipServe as the bsingle point of accountability /b for bon-time delivery, quality, and trial-level budget /b across assigned trials.
/p /lilipEnsure all btrial milestones, quality targets, and budget commitments /b are met.
/p /lilipProvide bbudget management and oversight /b at the trial level, including scenario planning and cost optimization.
/p /lilipReview and approve key bstudy-level documents /b (e.g., global master ICFs).
/p /lilipProactively identify, assess, and mitigate btrial-level risks /b , overseeing them through to closure.
/p /lilipDefine bprotocol deviation and resolution pathways /b .
/p /lilipTake ownership of bstudy-level escalations /b , including vendor performance issues and enrollment risks.




/p /lilipCommunicate trial risks, issues, changes, and milestones to relevant stakeholders in a timely and transparent manner.
/p /li /ul pRepresent Global Development (GD) at trial-level therapeutic area (TA) governance forums.
/p ullipContribute to and influence bgovernance decisions /b , ensuring operational feasibility and alignment.
/p /lilipAttend bClinical Team (CT) meetings /b when requested by the PDL.
/p /lilipEnsure strong alignment with key stakeholders on bprotocol amendments, enrollment targets, and study changes /b .
/p /li /ul pEnsure all btrial operational activities, TMF, and study documentation /b are bhealth authority–compliant /b , inspection-ready, and meet required quality standards at all times.
/p ulliSet up and oversee bclinical trial systems and documentation /b , including (but not limited to): E7 drivers, Safety Management Plan, JJAR Unified Clinical Trial Team (UCT) setup /li /ul h3Candidate Profile – Requirements /h3 ullipBachelor's degree (BS) or equivalent in bLife Sciences /b (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy) /p /lilipb6–8 years of clinical trial management experience /b within the pharmaceutical industry or a CRO, including specific therapeutic area experience /p /lilipProven experience managing clinical trials bend to end /b , from bstart-up through database lock and trial close-out /b /p /lilipStrong working knowledge of bICH-GCP /b , local laws, and regulatory requirements /p /lilipSuperior bclinical research operational knowledge /b with a demonstrated track record of delivery /p /lilipAbility to ensure ongoing bquality, compliance, and inspection readiness /b /p /lilipDemonstrated beffective leadership /b , with the ability to proactively guide study teams through key trial stages /p /lilipProven ability to bdelegate effectively /b while maintaining accountability /p /lilipExperience leading teams from bformation to high-performance /b /p /lilipStrong capability to manage bmultiple global stakeholders /b and cross-functional partners /p /lilipProven experience coordinating bglobal or regional teams in a virtual environment /b , for a minimum of b2 years (preferably 3+) /b /p /lilipAbility to foster team productivity, alignment, and cohesiveness across geographies /p /lilipStrong bproject planning and project management /b capabilities /p /lilipProven experience in bproactive planning /b , risk identification, and mitigation throughout the trial lifecycle /p /lilipAbility to gain bteam consensus on updated plans /b during changing project circumstances /p /lilipDemonstrated capacity for bindependent,



complex decision making /b /p /lilipSolution-oriented mindset with strong problem-solving skills /p /lilipStrong IT skills, including proficiency with bMicrosoft applications /b and familiarity with: Trial Master File (TMF) Iinical Trial Management Systems (CTMS) /p /lilipWillingness and ability to learn new systems and technologies /p /lilipMonitoring experience is recommended; other relevant experience (e.g., data management or central monitoring) will be considered /p /lilipExcellent bverbal and written communication skills /b , supporting effective collaboration /p /lilipProven experience developing bpresentations /b and presenting complex information to stakeholders /p /lilipStrong banalytical skills /b , with the ability to manage ambiguity when limited information is available /p /lilipAbility to understand, plan, and oversee bcountry- and vendor-level budgets /b /p /lilipAwareness of bcountry Out-of-Pocket (OOP) cost drivers /b and FTE-related cost components /p /lilipWillingness to btravel /b , as required /p /lilipProficiency in bEnglish /b (spoken and written) and the blocal country language /b , as applicable /p /li /ul pPlease note This role is not eligible for UK visa sponsorship /p pPlease note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered.
Any applications from candidates based outside of these locations will not be considered.
/p pIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Learn more at /p pIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
All information and credentials submitted in your application must be truthful and complete.
Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
We appreciate your honesty and professionalism.
/p pIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
We create connections that accelerate the development and commercialization of innovative medical treatments.
Everything we do is part of a journey to improve patient outcomes and population health worldwide.
/p pTo get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact.
No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.
Thank you for your interest in growing your career with us.
/p pEEO Minorities/Females/Protected Veterans/Disabled /p /p #J-*****-Ljbffr

📌 Global Trial Delivery Lead - Sponsor Dedicated (Milano)
🏢 Iqvia
📍 Milano