Study Delivery and Country Relations Manager

hace 1 semana


Barcelona, España IQVIA A tiempo completo

IQVIA’s Oncology Evidence Network (OEN) The Oncology Evidence Network (OEN) is a specialized team within IQVIA focused on delivering high-quality real‑world evidence (RWE) studies in oncology. We are an innovative and fast‑growing unit, our mandate is to build a network of cancer research centres to facilitate scientific studies on behalf of IQVIA’s pharma & biotech clients with a focus on oncology. These studies generate insights that directly contribute to access to novel treatments, better patient care and better patient outcomes for some of the most vulnerable patient groups. Within IQVIA, we play a pivotal role in supporting the broader IQVIA study business. We operate through a network of 35+ hospital groups and cancer centres across Europe, including key sites in the UK, Germany, France, Spain and Italy. Job Overview Country Lead for Spain (50%). You will be responsible for country‑level site engagement and site activations/start‑up, ensuring high quality and timely delivery across major real‑world evidence and oncology studies. You will act as the primary point of contact for Spanish sites and local stakeholders, coordinating closely with internal teams to unblock country critical paths and deliver on client commitments on time and on budget. Project Manager for OEN studies in Spain but also in other locations (50%). You will be responsible for study management tasks, support for feasibility assessment, ethics/contracting activities, and provide medical expertise to the broader OEN team. Essential Functions Lead country‑level execution in Spain: drive site engagement, feasibility, ethics/contracting, budget negotiations, site onboarding, and site activation and milestone timelines. Serve as the key point of contact for Spanish sites and country stakeholders; maintain proactive communications, manage issue logs/escalations, and sustain strong investigator relationships. Plan and track country start‑up: maintain country‑specific plans, risk registers, metrics and governance updates; ensure operational discipline and compliance with SOPs and sponsor expectations. Manage/lead consulting projects and multidisciplinary teams (internal and external) in the design, development and delivery of oncology studies. Leverage business experience to define strategic alternatives, structure approaches and prioritise analyses that answer client questions. Ensure clear, consistent communication across projects, within teams and with clients; follow up after delivery to ensure client satisfaction. Contribute to methodologies for future engagements; champion best practices for OEN country leadership and start‑up. Own proposal activities (preparation/modification) ensuring bid integrity and realistic country timelines/assumptions. Support business development by identifying follow‑on work and new leads tied to Spanish site capabilities and portfolio needs. Provide direction and thought leadership to clients and internal delivery teams; actively participate in team meetings and problem‑solving sessions. Develop high‑quality client deliverables (reports/presentations) and present significant portions of findings to senior stakeholders. Share subject matter expertise to elevate team capabilities and country start‑up excellence. Qualifications Master’s degree in life sciences/healthcare‑related field. 5+ years of professional experience in life science consulting, pharmaceutical industry or healthcare sector, with evidence of career progression. At least 2 years of experience in project management, ideally across multinational studies or country portfolios; demonstrable experience in site start‑up/activation and country‑level coordination strongly preferred. Oncology and/or RWE experience (in life sciences/healthcare) is a must. Fluency in both Spanish and English (spoken and written) is a must. Strong stakeholder management skills with client and site investigators. Strong analytical and problem‑solving skills; ability to translate country operational realities into pragmatic delivery plans. Excellent written and verbal communication; adept at presentations, meeting facilitation and business/report writing. Demonstrated ability to manage multiple projects and priorities, meeting deadlines with consistently high quality. Experience working in multi‑disciplinary, cross‑functional teams and leading staff. Ability to contribute to business development (lead identification, proposal development). Knowledge of consulting methodologies, tools and techniques; familiarity with Spanish ethics/RA pathways and site contracting is highly desirable. Willingness and ability to travel domestically (1–2 per month) and occasionally internationally. Permanent right to work in Spain. Please submit your CV in English IQVIA 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 https://jobs.iqvia.com. At IQVIA, we believe that diversity, inclusion and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi‑talented collaboration harnesses innovation to deliver superior outcomes. #J-18808-Ljbffr



  • Barcelona, España Novartis A tiempo completo

    *Role can be based in Madrid or Barcelona* The SSO Study Start-Up Team Lead is accountable for the governance and oversight of a study start-up team in a standalone country or OPC (operating country). The SSO Study Start-Up Team Lead is supporting the country/OPC SSU strategy and prioritization in close collaboration with SSU/OPC Head and Country/OPC LT to...


  • Barcelona, España AstraZeneca A tiempo completo

    **Location: Barcelona - On-Site** **Short role description** The GSM is a member of extended global study team supporting delivery of clinical studies within Late Development Oncology (LDO) to time, cost and quality, from Clinical Study Protocol (CSP)development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to...


  • Barcelona, España ADP A tiempo completo

    **Executive Relations Manager - Job Description** **I. Overview**: The ADP Global payroll team support the delivery of multi-country (International) Payroll Services across more than 140 countries. ADP's international payroll services are delivered through selected network of specialist partners (being both ADP and non-ADP) located within each local...

  • Country Lead Monitor

    hace 1 semana


    Barcelona, España Bayer A tiempo completo

    **Country lead monitor** **Position purpose** The CLM is accountable and responsible for overall country clinical trial activities in assigned studies. The CLM is a local team leader for the CRAs and oversees overall study progress for assigned studies within his/her country from country feasibility assessment through to study archive ensures country...


  • Barcelona, España AstraZeneca A tiempo completo

    **Location: Barcelona, Spain (On-site) / 3 days working from the office and 2 days working from home.** The Global Study Director (GSD) is a business-critical role within the Haematology organisation whose main accountability is the operational planning and delivery of high priority and complex clinical studies within a program, or across programs that are...


  • Barcelona, España AstraZeneca A tiempo completo

    **Location: Barcelona, Spain (on-site) 3 days working from the office and 2 days working from home.** The Global Study Associate Director (GSAD) is responsible for the delivery of clinical studies, including quality, timelines, budgets, resources, investigational sites, vendors, and key project deliverables in compliance with SOPs, Regulatory requirements...


  • Barcelona, España Amazon Spain Fulfillment, S.L.U. A tiempo completo

    Proven track record of accomplishments in a fast paced similar environment to Amazon FCs/AMZL - Fluent in Spanish and English - Demonstrate problem solving and analytical capability. - Extensive knowledge of employment law. - Demonstrate ability to motivate others and influence work behaviors - Strong negotiation and influencing skills - Extensive experience...

  • Local Trial Manager

    hace 6 días


    Barcelona, España Amgen A tiempo completo

    **HOW MIGHT YOU DEFY IMAGINATION?** If you feel like you’re part of something bigger, it’s because you are! At Amgen, our shared mission—to serve patients—drives all that we do, which is the key for us to becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together by researching, manufacturing,...

  • Expert Country Partner

    hace 6 días


    Barcelona, España Bayer A tiempo completo

    **At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our...


  • Barcelona, España AstraZeneca A tiempo completo

    The Global Study Associate Manager (GSAM) is a pivotal role within Development Operations, integral to the global study team. This position supports the delivery of clinical studies from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, and the development of Clinical Study Reports (CSR) to study archiving. The GSAM...