Cell Therapy - Field Clinical Advisor

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/89m678

pAre you ready to turn cutting-edge cell therapy science into real-world trial performance and meaningful patient impact? /p pAs the field-facing scientific and clinical expert, you will accelerate study execution and retention, sharpen safety practices, and enable early insight generation that shapes how we run our trials. Your work will translate complex protocols into practical, consistent actions across diverse sites and indications, driving measurable improvements in feasibility, start‑up, and conduct. /p pYou will collaborate closely across functions to advance a bold pipeline with speed and quality, connecting therapeutic innovation to the day‑to‑day realities of study teams and trialists. Picture yourself guiding trialists through the cell therapy patient journey, elevating site performance, and transforming field insights into decisions that improve how we design, run, and scale studies. How would you turn evidence into action and help trial sites deliver with clarity and confidence? /p h3Accountabilities /h3 ul liCell Therapy Expertise: Build and continuously maintain deep knowledge across indications and assets; be the go‑to expert who shapes guidance, training, and best practices that raise execution quality and consistency. /li liStrategic Communication: Lead clear, compliant communications that convey strategy, portfolio breadth, and product differentiation; align messaging across regions to ensure consistency for assigned protocols and sites. /li liSite Readiness and Training: Support and deliver site initiation content and advanced protocol education; implement competency‑based training to drive readiness, shorten start‑up timelines, and improve protocol adherence. /li liEnrollment Optimization: Translate inclusion/exclusion criteria and patient flow into pragmatic site actions that raise enrolment rates, reduce screen failures, and minimize attrition. /li liInsight Generation and Continuous Improvement: Capture and synthesize field insights on feasibility, bottlenecks, and patient pathways; support protocol and process adjustments and drive preventive actions to reduce deviations and data queries. /li liLocal Initiatives and Scaling: Co‑create and implement high‑impact local initiatives with trialists and key experts; track outcomes and scale successful approaches aligned to program priorities for broader impact. /li liScientific Engagement and Governance: Facilitate timely, high‑quality scientific dialogues with investigators and internal partners; capture learnings and ensure governance compliance. /li liCross‑Functional Coordination and Service: Coordinate with Clinical Operations, Clinical Development, Medical Affairs,



Supply/Logistics, Patient Operations, and Country teams to provide rapid, reliable service to study sites; /li liCompliance and Regulations: Maintain current knowledge of local regulations, guidelines, and internal policies; translate requirements into site actions to support inspection readiness. /li liExternal Engagement and Innovation: Attend relevant scientific meetings; synthesize and share insights. Build relationships across the ecosystem to identify, pilot, and scale innovations that shorten cycle times, improve quality, and enhance site experience. /li liCountry Strategy and Governance Alignment: Provide country‑specific field insights to priority initiatives; shape strategies and deliverables for scalable, locally compliant adoption. Partner with Medical Affairs on scientific plans and field content; coordinate within governance to reflect market dynamics, ensuring traceability from field signals to decisions and operating within policies and SOPs. /li /ul h3Essential Skills/Experience /h3 ul liEducation: Bachelor’s degree in a health‑related field required; advanced degree (PharmD, PhD, MSc, NP/PA, MD/RN) preferred. /li liStrong prior experience in clinical research or field‑facing roles within oncology/hematology or advanced therapies; direct cell therapy experience strongly preferred. /li liWorking knowledge of GCP, clinical trial operations, and cell therapy patient journey. /li liExcellent stakeholder management, presentation, and training skills; ability to translate complex protocols into practical site actions. /li liWillingness to travel regionally/nationally and internationally to support sites and program needs. /li liPatient- and site‑centric mindset with a bias for action and problem solving. /li liData informed approach to identify trends, risks, and opportunities for operational improvement. /li liAgility to support multiple studies and indications in a dynamic portfolio environment. /li /ul h3Desirable Skills/Experience /h3 ul liPrior ownership of site performance metrics. /li liPrior account leadership and existing relationships in C/D suites. /li liProven ability to lead trainings, influence without authority, and translate complex protocols into pragmatic site actions,



adept at concise escalation and stakeholder alignment. /li liPrior large pharma experience in cell therapy. /li liScientific training and/or protocol training expertise. /li /ul h3We offer: /h3 pSalary range: 90.589,60€ - 135.884,40€ per annum /p pContract Level: Dirigente /p pCBA: Chemical-Pharmaceutical /p pFull‑time /p pPermanent position /p pField base role: Italy /p h3Benefits: /h3 ul liAn annual target premio governed by the Company’s policies as amended from time to time and subject to periodic review/Sales incentives governed by the Company’s policies as amended from time to time and subject to periodic review /li liWellbeing benefits (welfare, insurance, psychological support, etc.) governed by the Company’s policies as amended from time to time and subject to periodic review /li liCompany Car governed by the Company’s policies as amended from time to time and subject to periodic review /li /ul pFinal compensation will be determined based on a variety of factors, including but not limited to skills, experience, internal organizational equity and other relevant factor. /p pWe carefully consider all applications, including those from candidates eligible under Italian Protected Categories legislation (Art. 1 and Art. 18, L. 68/99). /p h3Why AstraZeneca: /h3 pJoin a team advancing one of the most ambitious oncology pipelines, where cell therapy innovation and decisive science meet real patient needs. You will work with novel modalities and data‑rich programs, partnering across disciplines that put unexpected teams in the same room to unleash bold thinking. We value kindness alongside ambition and empower people to communicate bravely, challenge the norm, learn fast, and turn insights into action. Your field expertise will directly shape how we generate evidence and run studies, tying rigorous execution to outcomes that matter for patients and for the future of cancer treatment. /p h3Date Posted /h3 p02-ott-2026 /p h3Closing Date /h3 p16-ott-2026 /p pAstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry‑leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non‑discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. /p #J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/89m678