Associate Director – Clinical Project Management

IQVIA

Associate Director responsible for managing clinical project operations for IQVIA Biotech. Ensuring study execution and compliance while driving strategic leadership with customers.

Posted 7/30/2026full-timeLisbon • 🇵🇹 PortugalSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in clinical research project management, including the development of integrated study management plans and proactive stakeholder communication. Proficient in identifying quality risks and mentoring junior team members to achieve project objectives.

Highest-signal resume keywords

Clinical Research ExperienceProject Management ExperienceKnowledge of Clinical TrialsICH GCP ComplianceStrong Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchProject ManagementStudy Management PlansQuality Risk ManagementRegulatory Requirements

Soft Skills

Problem SolvingPlanningTime ManagementPrioritizationCoaching

Tools & Technologies

MS Office Applications

Industry Keywords

Clinical TrialsRegulatory ComplianceLocal LawsResearch Guidelines

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Manage and support the operational elements and execution of studies and/or programs
Develop and/or support on the preparation of integrated study management plans in collaboration with the core project team
Serve as primary project oversight and/or contact with customers
Monitor progress against contract and prepare/present project information proactively to all stakeholders
Coach and/or mentor junior team members
Achieve project quality by identifying and proactively managing quality risks and issues

Requirements

What you’ll need

Bachelor's Degree Life sciences or related field
Requires 10 years clinical research experience including 6 years of project management experience
Knowledge of clinical trials - Knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines
Strong written and verbal communication skills
Strong problem solving skills
Planning, time management and prioritization skills
Good software and computer skills, including MS Office applications

Benefits

Comp & perks

Professional development
Health insurance
Flexible working arrangements