Senior Global Trial Manager – Late-Phase Studies

IQVIA; Madrid; On-site; EUR 90,000 - 120,000; Full time

Job summary

IQVIA is seeking a Senior Global Trial Manager for the Single Sponsor Department in Madrid. You will lead late-phase global trials, collaborate with Medical Affairs, study teams and external partners to meet timelines, budgets and quality standards.

This role offers exposure to multiple pathways (SRC, NIS, MAP, IITs, RCs, PLD) and requires strong regulatory documentation experience. UK visa sponsorship is not available. Based in Madrid with global scope.

Qualifications

• Must have 5+ years planning, executing and reporting global clinical trials in pharma/CRO.
• Experience in global, cross-functional matrix teams with internal and external stakeholders.
• Ability to manage multiple studies/projects in parallel while meeting time, budget and quality targets.
• Strong planning, communication, influencing and problem-solving skills.
• Experience contributing to clinical study documents (protocols, PSURs, DSURs).

Responsibilities

• Plan, coordinate and oversee Medical Affairs activities from setup through closure, ensuring milestones meet quality standards.
• Act as the operational point of contact for assigned work and build relationships with global stakeholders.
• Develop and maintain study, program and regulatory documentation with required inputs and approvals.
• Coordinate inputs for program-level and safety documents (DSURs, PSURs, Investigator Brochures).
• Organise kick-off, strategy, governance meetings; prepare pre-reads, agendas and minutes.
• Monitor trackers, budgets and resources; report progress and dependencies.

Skills

Strategic planning

Global trial management

Stakeholder management

Budgeting and resourcing

Cross-functional collaboration

Regulatory documentation

Education

Advanced degree in life sciences or healthcare

Job description

IQVIA is seeking a Senior Global Trial Manager for the Single Sponsor Department in Madrid. You will lead late-phase global trials, collaborate with Medical Affairs, study teams and external partners to meet timelines, budgets and quality standards.

This role offers exposure to multiple pathways (SRC, NIS, MAP, IITs, RCs, PLD) and requires strong regulatory documentation experience. UK visa sponsorship is not available. Based in Madrid with global scope.