Global Clinical Study Lead, Operations

IQVIA; Warszawa; On-site; PLN 172,000 - 405,000; Full time

Job summary

IQVIA Warsaw seeks a Global Study Manager to support delivery of clinical studies within BioPharmaceuticals Clinical Operations. This role collaborates across teams and with CROs to ensure on-time, on-budget, high-quality study execution from CSP through CSR and archiving.

The candidate will maintain study documents, assist with budgets, and manage external partners while adhering to global processes and ICH/GCP standards. Strong English and leadership are essential.

Qualifications

• University degree in medical or biological sciences or related field.
• 3+ years experience in pharmaceutical or clinical operations.
• Solid knowledge of ICH/GCP guidelines.
• Strong communication, relationship-building and leadership skills.

Responsibilities

• Lead preparation of delegated study documents and supplier-related docs.
• Coordinate with internal and external partners to ensure timely study delivery.
• Support budgeting, invoices, and adherence to quality standards.
• Participate in study planning, meetings and risk mitigation activities.
• Ensure study documents are complete and QA verified in TMF.

Skills

Communication skills

Leadership

Project management

English proficiency

Independent worker

Team collaboration

Computer skills

Education

University degree in medical/biological sciences or related

Tools

Microsoft Office

Job description

IQVIA Warsaw seeks a Global Study Manager to support delivery of clinical studies within BioPharmaceuticals Clinical Operations. This role collaborates across teams and with CROs to ensure on-time, on-budget, high-quality study execution from CSP through CSR and archiving.

The candidate will maintain study documents, assist with budgets, and manage external partners while adhering to global processes and ICH/GCP standards. Strong English and leadership are essential.