Trial Delivery Leader (TDL) The Trial Delivery Leader (TDL) serves as the single point of accountability for trial operational strategy, trial‐level budget, quality, and on‐time delivery of assigned clinical trials. The TDL works in close partnership with the Program Delivery Leader (PDL) and co‐leads the Cross‐Functional Trial Team (CFTT) to ensure trial strategies are aligned with program objectives and executed efficiently. The Trial Delivery Leader plays a critical role in ensuring clinical trials are delivered efficiently, compliantly, and with high quality, while balancing speed, cost, and innovation. trial endpoints, ARBM, biomarkers, DEICT, digital health, companion diagnostics) Ensuring timely delivery of trial‐level deliverables Early operational input during initial protocol development Development of cost‐optimized and accelerated scenarios and innovative approaches, aligned with trial tiering (post‐POC) Develop the trial operational strategy, integrating and aligning all trial‐level functional strategies into a single, holistic approach, including vendor strategy. Serve as the single point of accountability for on‐time delivery, quality, and trial‐level budget across assigned trials. Provide budget management and oversight at the trial level, including scenario planning and cost optimization. Represent Global Development (GD) at trial‐level therapeutic area (TA) governance forums. Ensure all trial operational activities, TMF, and study documentation are health authority‐compliant, inspection‐ready, and meet required quality standards at all times. Set up and oversee clinical trial systems and documentation, including (but not limited to): E7 drivers, Safety Management Plan, JJAR & Unified Clinical Trial Team (UCT) setup. Bachelor's degree (BS) or equivalent in Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing,



Pharmacy)6–8 years of clinical trial management experience within the pharmaceutical industry or a CRO, including specific therapeutic area experience Proven experience managing clinical trials end to end, from start‐up through database lock and trial close‐out Strong working knowledge of ICH‐GCP, local laws, and regulatory requirements Superior clinical research operational knowledge with a demonstrated track record of delivery Ability to ensure ongoing quality, compliance, and inspection readiness Demonstrated effective leadership, with the ability to proactively guide study teams through key trial stages Experience leading teams from formation to high‐performance Proven experience coordinating global or regional teams in a virtual environment, for a minimum of 2 years (preferably 3+) Ability to foster team productivity, alignment, and cohesiveness across geographies Strong project planning and project management capabilities Proven experience in proactive planning, risk identification, and mitigation throughout the trial lifecycle Ability to gain team consensus on updated plans during changing project circumstances Strong IT skills, including proficiency with Microsoft applications and familiarity with Trial Master File (TMF) & Trial Management Systems (CTMS) Willingness and ability to learn new systems and technologies Monitoring experience is recommended; other relevant experience (e.g., data management or central monitoring) will be considered Excellent verbal and written communication skills, supporting effective collaboration Proven experience developing presentations and presenting complex information to stakeholders Strong analytical skills, with the ability to manage ambiguity when limited information is available Awareness of country Out‐of‐Pocket (OOP) cost drivers and FTE‐related cost components Proficiency in English (spoken and written) and the local country language, as applicable This role is not eligible for UK visa sponsorship

📌 IT Delivery Lead (Turbigo)
🏢 Altro
📍 Turbigo