Cell Therapy Field Clinical Advisor job opportunity at AstraZeneca.



DateMore Than 30 Days Ago bot
AstraZeneca Cell Therapy Field Clinical Advisor
Experience: 5-years
Pattern: full-time
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degreePhD
loacation Spain - Barcelona, Spain
loacation Spain - Barcel..........Spain

Introduction to the role Cell Therapy Field Clinical Advisors (FCAs) are part of the Global Cell Therapy Clinical Operations team and play a critical role in the successful execution of cell therapy clinical trials—driving recruitment ,   retention   and safety management   while enabling early insight generation. FCAs focus   on   clinical study protocol   expertise   and education ,   optimizing   the patient journey, and   cell therapy   pipeline engagement . The role requires close collaboration with   other CTCO Functions,   Clinical Development, and Medical Affairs across multiple indications and business units to advance AstraZeneca’s diverse cell therapy portfolio. Typical Accountabilities   Scientific Expertise and Education    Pipeline Mastery at Scale: Build and continuously   maintain   deep knowledge of AstraZeneca’s cell therapy pipeline across multiple indications and   assets.     Recognized Thought Leadership:   Establish   and sustain highest-level scientific and medical   expertise   in cell   therapy; recognized   internally and externally as a go-to expert, shaping guidance,   training , and best practices for assi gned protocols and sites   Strategic Portfolio Communication: Lead site-facing and expert stakeholder communications that clearly convey AstraZeneca’s cell therapy strategy, portfolio breadth, and product differentiation; ensure consistent, compliant messaging across regions.   Initiative Ownership and Execution: Design, lead, and implement high-impact local initiatives with trialists and key experts to support R&D or study implementation, aligned with GPT, Global R&D, and Country Medical Affairs; track outcomes and scale successful approaches.   Education Gap Identification and Closure: Systematically assess educational needs across owned sites, deliver advanced   protocol   training , and escalate patterns to Global Clinical Development with recommendations for enterprise-level solutions.   Insight Generation and Influence: Capture, synthesize, and deliver actionable field insights (feasibility, operational bottlenecks, patient pathways) to global and local stakeholders; drive early risk identification and influence protocol/process adjustments .     Clinical Trial Support   Advanced Education and Readiness : Lead delivery of SIV content; provide advanced protocol education and competency-based staff training to ensure readiness, compliance, and consistency across sites and indications.   D rive patient selection quality, safety management, and site-specific action plans ;   deliver measurable improvements in start-up timelines and protocol adherence   Recruitment and Retention Performance : Implement targeted   protocol   education   (e.g., inclusion/exclusion criteria application   etc. )   to   uplift   enrolment   rates, reduce screen failures, and minimize attrition.   Issue Triage, Escalation, and Risk Mitigation : Serve as the primary field point for   protocol and   clinical issues; triage and escalate appropriately, drive root-cause analysis, and implement corrective/preventive actions to reduce deviations and data queries.   Structured, Compliant Scientific Exchange : Lead   timely , high-quality scientific and medical communications with trialists and internal partners, ensuring alignment with compliance policies and legal requirements; standardize messaging and capture learnings for reuse.   Insight Loop and Continuous Improvement : Systematically capture site-level insights; synthesize trends for study teams and cross-functional stakeholders, influencing protocol/process adjustments and scaling proven practices.       Operational    Cross-functional orchestration: Lead coordinated delivery with   CTCO Functions,   Clinical Development, Medical Affairs, Supply/Logistics,   Patient Operations   and   Country Ops   to ensure rapid, reliable service to internal stakeholders and study sites .   Portfolio coverage and resiliency: Provide proactive coverage for other FCAs and high-priority sites; implement standardized playbooks to   maintain   continuity of operations during surges, vacations, or escalations.   Regulatory and policy stewardship:   Maintain   current knowledge of local regulations, guidelines, codes of practice, and AstraZeneca policies relevant to Clinical Development; translate requirements into practical site actions and support inspection readiness.   External scientific engagement: Attend and contribute at relevant scientific meetings and conferences; synthesize takeaways into concise briefs and recommendations for study teams and operational processes.   Innovation sourcing and scaling: Build relationships with industry leaders and ecosystem partners;   identify , pilot, and scale innovations (e.g., workflow tools,   logistics   optimizations, patient support solutions) that improve cycle times, quality, and site experience.   Cross Functional   Global   workstreams : Provide   country specific   field insights and subject-matter   expertise   to priority global initiatives; review/shape core strategies and deliverables to enable scalable, locally compliant adoption.   Medical Affairs: Partner on scientific strategy, congress/education plans, and field content; ensure accuracy, balance, and   governance   compliance across materials and training.   Commercial (within governance): Coordinate through approved interfaces to align on market dynamics   and   objectives   Evidence and insights: Elevate actionable field signals to inform global   research   strategy and lifecycle plans; ensure traceability from signal to decision.   Governance:   Operate   within AZ policies/SOPs and local regulations   Impact   Operational velocity and quality: Directly improve speed, quality, and consistency of AstraZeneca’s cell therapy trials—reducing cycle times, elevating protocol adherence, and accelerating patient access to innovative treatments. Education, Qualifications,   Skills   and Experience Essential Education : Bachelor’s degree in a health-related field   required ; advanced degree (PharmD, PhD, MSc, NP/PA, MD/RN) preferred.   Experience : 5+ years in clinical research or field-facing roles within oncology/ hematology   or advanced therapies; direct cell therapy experience strongly preferred.   Technical Skills :   Concentrated   understanding of GCP, clinical trial operations, and cell therapy   patient journey   Collaboration and Communication : Excellent stakeholder management, presentation, and training skills; ability to translate complex protocols into practical site actions.   Travel :   Willingness to   travel   regionally/nationally   a nd   internationally to support sites and program needs.   Patient- and site-centric mindset with a bias for action and problem solving.   Data-informed approach to   identify   trends, risks, and opportunities for operational improvement.   Agility to support multiple studies and indications in a dynamic portfolio environment. Desirable 5–8+ years in clinical research or field-facing roles, ideally in oncology/ hematology /immunology/rare disease   and/or advanced therapies; direct CAR-T/Cell Therapy experience strongly preferred.    Prior ownership of site performance metrics    Prior account leadership   and existing relationships in C/D suites   Proven ability to lead trainings, influence without authority, and translate complex protocols into pragmatic site   actions,   adept at concise escalation and stakeholder alignment.    Prior large pharma experience in cell therapy   Scientific training and/or protocol training   expertise   Date Posted 27-ene-2026 Closing Date 13-feb-2026 AstraZeneca 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.

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