Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)

IQVIA

Pharmaceutical Research Industry

Madrid - Spanien

Manager / Team Leader

Hybrid

Experteer Overview

As Associate Director Senior Study Lead, you guide cross-functional clinical trial teams to plan and run studies end-to-end, ensuring proactive risk-aware execution. You drive study budget and staffing, and promote operational excellence through process improvements and knowledge sharing. You work within a matrixed environment to deliver high-quality protocols, reports, and study deliverables. This role offers impact across global studies and the chance to shape how we accelerate patient access to medicines.

Compensation / Benefits

home-based
remote work
collaborative tools
global team
autonomy and balance

Responsibilities

Lead and deliver clinical studies with informed study-level decisions
Act as CTT product owner with defined agile duties
Engage as an active member of the Clinical Operations community
Promote operational excellence in protocol development, study reports, and related documents
Oversee patient recruitment, data, documentation, and CSR delivery
Ensure timely, quality delivery of protocol, ICF, Monitoring Plan, and CSR
Manage study budget and resource allocation
Implement proactive, iterative planning with risk contingencies in a global, matrix context

Key requirements

Bachelor in Life Sciences (advanced degree strongly preferred)
4 years of recent clinical research or drug development experience across Phases I–IV
3 years of global/matrix study execution experience in pharma or CRO with GCP/ICH and FDA/EMA knowledge
Experience managing people in a global, matrix environment; virtual team leadership
Strong stakeholder relationships, negotiation, and conflict resolution
Excellent verbal and written communication; fluent English
Location: home-based; not eligible for UK visa sponsorship

excellent communication and presentation strong negotiation and conflict resolution collaboration across cross-functional teams GCP/ICH knowledge FDA/EMA familiarity global study planning and budgeting

Description

As Associate Director Senior Study Lead, you guide cross-functional clinical trial teams to plan and run studies end-to-end, ensuring proact…

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