Global Study Manager Early Oncology
Posted date Jun. 10, 2026
Contract type Full time
Job ID R\-253807
Why choose AstraZeneca Spain?
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AstraZeneca Spain is a rising force in our global business. With headquarters in Madrid and our global hub in Barcelona, we’ve become an important international centre of excellence in the fight against critical disease. Boasting vibrant universities and business schools, the Barcelona ecosystem is a place where scientists can thrive. We attract a diverse workforce from across the globe, shining a beacon for innovation in a country that’s committed to clinical development.
We invite you to bring your talents to Barcelona where our respiratory medicine R\&D and Global Marketing centre offers opportunities in R\&D, IT, Commercial and HR. Or join us in Madrid and shape our growth in our BUs (Respiratory, Oncology \& CVRM ), and a range of Corporate functions. Additionally, you can find sales roles throughout the country. Together, we’re contributing to a world\-leading pipeline of therapeutics and delivering life\-changing medicines to patients.
Who do we look for?
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Calling all tech innovators, ownership takers, challenge seekers and proactive collaborators. At AstraZeneca Spain, breakthroughs born in the lab become transformative medicine for the world's most complex diseases. Alongside technical expertise, colleagues have the resilience, energy and collaborative mindset to change lanes, work with different teams and start projects from scratch.
Here, diverse minds and bold disruptors can meaningfully impact the future of healthcare using cutting\-edge technology. Whether you join us in Madrid or Barcelona, you can make a tangible impact within a global biopharmaceutical company that invests in your future. Join a talented global team that's powering AstraZeneca to better serve patients every day.
Success Profile
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Ready to make an impact in your career? If you're passionate, growth\-orientated and a true team player, we'll help you succeed. Here are some of the skills and capabilities we look for.
Diverse collaborators
This is a speak\-up culture that values collaboration. You’ll proactively bring your unique perspectives, experiences and skills to the table and seek the same from others. With our international team composition and the need for fast\-paced collaboration, you’ll always be building new connections with colleagues.
Cutting\-edge innovators
When you join us, you’ll be part of a team that embraces digital technology and data to transform the way we work and the work we do. Every day, you’ll help make history, empowered to ignite your creativity and build something enduring.
Resilient trailblazers
Here, the answers aren’t always available. So, you’ll need to bring a fearless, self\-starter mindset to navigate uncharted territories. You’ll harness your ceaseless energy to discover and make the necessary connections with colleagues to shape the future and achieve maximum impact.
Agile movers
Seize ownership and excel with autonomy to enjoy the constant rush of ground\-breaking discovery. Your ability to anticipate sudden shifts and adapt swiftly will prove critical as you make your mark in an environment that rewards initiative and resilience.
Responsibilities
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Job ID R\-253807 Date posted 06/10/2026
Are you ready to run global oncology studies at pace and turn rigorous science into operational reality for patients sooner? In this role, you will orchestrate complex, multi\-country trials from protocol through Clinical Study Report, ensuring quality and compliance while unblocking the path to decisive data.
You will join a fast\-moving, empowered team that brings together study operations, data management, patient safety, supply chain, and regulatory experts to deliver high\-quality studies across multiple countries. Expect to make clear decisions, challenge constructively, and take smart, evidence\-based risks to accelerate outcomes. How will you use your vendor leadership and ICH\-GCP expertise to deliver clean data faster and raise the bar on inspection readiness?
Accountabilities:
- Study Document Leadership: Drive the development, updates and amendments of core study documents, ensuring template and version compliance from start\-up through closeout.
- Country Start\-up and Submissions: Lead country\-specific agreements, confidentiality agreements and clinical trial applications to enable rapid site activation across multiple geographies.
- Vendor Strategy and Oversight: Set up and manage third\-party vendors, assess statements of work and budgets, oversee change orders, and ensure partners deliver to quality, timeline and cost.
- Data Delivery Enablement: Provide input to data management documents (e.g., CRF, data validation specifications) and partner with data management and sites to facilitate timely, high\-quality data.
- Budget and Contracts Management: Initiate contract and budget requests, track status and deliverables, raise purchase orders, review invoices, and monitor spend against approved budgets.
- Supply and Materials Coordination: Secure investigational product and study materials by liaising with internal supply teams and external service providers to maintain uninterrupted trial conduct.
- Recruitment, Risk and Quality Oversight: Provide oversight of site and vendor performance, support recruitment and data delivery plans, and implement risk mitigation strategies to safeguard timelines and quality.
- Insurance and Regulatory Support: Assist with clinical trial insurance processes, tracking approvals, revisions and renewals to maintain coverage.
- Study Progress Monitoring: Monitor conduct and progress, proactively identifying and resolving issues that could impact quality, timelines or budget and escalating when needed.
- TMF Excellence and Inspection Readiness: Support set\-up, maintenance, closeout and archiving of the Trial Master File, maintaining continual inspection readiness.
- Communications and Stakeholder Engagement: Prepare clear, concise materials for meetings, newsletters and internal portals to align stakeholders and sustain momentum.
- Audit and Inspection Preparation: Support the study team through audits and regulatory inspections, ensuring robust responses and sustained compliance.
- OP and Process Improvement: Contribute to reviews of new or updated SOPs and guidance documents, sharing learnings from studies to improve ways of working. Essential
- University degree / Bachelor’s degree, preferably in medical or biological science, or discipline associated with Clinical Research, or equivalent experience Minimum of 3\-4 years of progressive clinical trial experience
- Experience of working with and delivering through strategic partners and 3rd party vendors \- Excellent knowledge of ICH\-GCP principles
- Team orientated
- Ability to coordinate and prioritise multiple tasks and deliverables
- Proactive approach
- High degree of flexibility
- Demonstrated verbal and written communication skills
- Good negotiation and collaboration skills
- Demonstrated interpersonal and problemsolving skills
- Some travel may be required
- Early phase oncology clinical trial experience
- Global study management experience
Call to Action: Own the delivery of studies that can reshape cancer care—bring your leadership to the table and advance the next breakthrough with us today!
Date Posted
09\-jun\-2026
Closing Date
29\-jun\-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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Reasons to Join
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Thomas Mathisen
There are many things I enjoy when working at AstraZeneca, mainly the Speak up culture, the great colleagues that are in my teams, the great products that AstraZeneca provides to our patients and the challenging conversations I have around our medicines.
Sales Representative Oslo, Norway
There are many things I enjoy when working at AstraZeneca, mainly the Speak up culture, the great colleagues that are in my teams, the great products that AstraZeneca provides to our patients and the challenging conversations I have around our medicines.
Christine Recchio
Working at AstraZeneca has impacted my life in such a positive way. I now have an improved work\-life balance through creating my own schedule and time management, I feel a balance that I
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