20 publicaciones de empleo destacadas de delivery lead sponsor en la moraleja, md (¡Están contratando!)

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- Jornada completa
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Celonis —Madrid, Madrid provincia
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Cencora —Madrid, Madrid provincia
- Jornada completa
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Amazon EU SARL (Spain Branch) —Madrid, Madrid provincia
- Jornada completa
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Allucent —Madrid, Madrid provincia
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CRA I-II in Madrid. Sponsor dedicated.
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IQVIA —Madrid, Madrid provincia
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TK ELEVATOR IBERICA HOLDING, S.L. UNIPERSONAL. —Madrid, Madrid provincia
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- Teletrabajo
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- Inglés
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Global Trial Delivery Lead - Sponsor Dedicated

IQVIA -
Madrid, Madrid provincia

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Detalles del empleo

Jornada completa

Beneficios

Teletrabajo opcional

Cualificaciones

Investigación clínica
Inglés
Investigación
Máster
Programación orientada a objetos
Project management
Grado
Optimización de la conversión
Habilidades de comunicación

Descripción completa del empleo

Madrid, Spain | Full time | Home-based | R1539797

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. This role represents the evolution of the Global Trial Leader (GTL), with a stronger emphasis on strategic leadership, end-to-end accountability, and governance-level decision making.

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. By serving as the single point of accountability, the TDL enables clearer decision making, stronger execution, and improved trial outcomes across the development portfolio

Scope of Focus

The Trial Delivery Leader is primarily focused on strategic leadership and execution oversight, rather than administrative task execution. Key focus areas include:

Co-leading the CFTT and driving cross-functional alignment
Coordinating functional strategies (e.g., trial endpoints, ARBM, biomarkers, DEICT, digital health, companion diagnostics)
Ensuring timely delivery of trial-level deliverables
Trial-level budget ownership and oversight
Quality oversight and inspection readiness
Early operational input during initial protocol development
Development of cost-optimized and accelerated scenarios and innovative approaches, aligned with trial tiering (post-POC)

Key Accountabilities

Develop the trial operational strategy, integrating and aligning all trial-level functional strategies into a single, holistic approach, including vendor strategy.
Partner closely with the PDL to shape trial-level strategy in alignment with overall program strategy.
Co-lead the Cross-Functional Trial Team (CFTT), setting meeting cadence, agendas, and expectations.
Empower CFTT members to independently drive their functional deliverables while maintaining accountability for timelines and quality.
Serve as the single point of accountability for on-time delivery, quality, and trial-level budget across assigned trials.
Ensure all trial milestones, quality targets, and budget commitments are met.
Provide budget management and oversight at the trial level, including scenario planning and cost optimization.
Review and approve key study-level documents (e.g., global master ICFs).
Proactively identify, assess, and mitigate trial-level risks, overseeing them through to closure.
Define protocol deviation and resolution pathways.
Take ownership of study-level escalations, including vendor performance issues and enrollment risks.
Communicate trial risks, issues, changes, and milestones to relevant stakeholders in a timely and transparent manner.
Represent Global Development (GD) at trial-level therapeutic area (TA) governance forums.
Contribute to and influence governance decisions, ensuring operational feasibility and alignment.
Attend Clinical Team (CT) meetings when requested by the PDL.
Ensure strong alignment with key stakeholders on protocol amendments, enrollment targets, and study changes.
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

Candidate Profile – Requirements

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
Proven ability to delegate effectively while maintaining accountability
Experience leading teams from formation to high-performance
Strong capability to manage multiple global stakeholders and cross-functional partners
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
Demonstrated capacity for independent, complex decision making
Solution-oriented mindset with strong problem-solving skills
Strong IT skills, including proficiency with Microsoft applications and familiarity with: Trial Master File (TMF) & Iinical 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
Ability to understand, plan, and oversee country- and vendor-level budgets
Awareness of country Out-of-Pocket (OOP) cost drivers and FTE-related cost components
Willingness to travel, as required
Proficiency in English (spoken and written) and the local country language, as applicable

Please note This role is not eligible for UK visa sponsorship

Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered.

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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Quiero recibir la alerta de empleo más reciente de delivery lead sponsor en la moraleja, md

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Scope of Focus

Key Accountabilities

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.

Candidate Profile – Requirements

Where you'll work

Home-based

Culture

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