Global Study Manager – Single Sponsor, EMEA

IQVIA

. Support delivery of clinical studies from Clinical Study Protocol development through study set-up, maintenance, close-out, Clinical Study Report development, and study archiving .

Posted 10/14/2026full-timeWarsaw • PolandMid-LevelSenior💰 PLN 171,500 - PLN 404,600 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical study management, including protocol development, compliance with ICH/GCP guidelines, and effective collaboration with internal teams and external service providers. Proficient in project management and budget oversight within the pharmaceutical industry.

Highest-signal resume keywords

Clinical Study ManagementICH/GCP GuidelinesProject ManagementExternal Service Provider ManagementClinical Development Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study Protocol DevelopmentTrial Master File MaintenanceBudget ManagementRisk Identification and MitigationInvestigational Product Supply Management

Soft Skills

Excellent Communication SkillsRelationship BuildingCollaborationLeadership

Tools & Technologies

Computer ProficiencyAdvanced Computer Skills

Industry Keywords

Pharmaceutical IndustryClinical ResearchDrug Development ProcessQuality Compliance

About the role

Key responsibilities & impact

Support delivery of clinical studies from Clinical Study Protocol development through study set-up, maintenance, close-out, Clinical Study Report development, and study archiving
Lead or contribute to delegated study documents and external service provider-related documents
Maintain and facilitate interactions with internal functions, CROs, and other external service providers
Contribute to planning and conducting internal and external meetings
Ensure supply of investigational product and study materials
Contribute to risk and issue identification and mitigation/action plans
Ensure study documents are complete, quality-verified, and maintained in the Trial Master File
Support budget management, including external service provider invoice reconciliation
Follow global clinical processes, quality and compliance requirements, and ICH/GCP guidelines
Support the Global Study Director and/or Global Study Associate Director with project management
Support CRO Project Manager oversight for outsourced studies
Take on process improvement and non-drug project assignments

Requirements

What you’ll need

University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research
Relevant experience from within the pharmaceutical industry or similar organization or academic experience, preferably of at least 3 years
Knowledge of clinical development / drug development process in various phases of development and therapy areas
Excellent knowledge of international guidelines ICH/GCP
Excellent communication and relationship building skills, including external service provider management skills
Good project management skills
Demonstrated ability to collaborate as well as work independently
Demonstrated leadership skills
Computer proficiency, advanced computer skills in day-to-day tasks
Excellent verbal and written communication in English
Only candidates based in Warsaw, Poland; Barcelona, Spain; or Madrid, Spain will be considered
This role is not eligible for UK visa sponsorship

Benefits

Comp & perks

Health and welfare benefits
Incentive plans, bonuses, and/or other forms of compensation may be offered