Lead Clinical Data Management – Hybrid Role

GSK; Warszawa; Hybrid; PLN 256,000 - 426,000; Full time

Job summary

GSK in Poland is seeking an experienced professional to lead end-to-end clinical data management across multiple studies. You will drive data quality, timelines and regulatory compliance while coordinating with study teams and external partners.

You will oversee data capture tools (eCRF, eCOA) and data flow, ensuring clean databases and timely database locks. This role offers growth within a global biopharma environment and hybrid work arrangements in Poland.

Qualifications

• Bachelor’s degree in a scientific, clinical, data or computer-related discipline.
• Minimum of 4 years’ experience in clinical data management or clinical trials in pharma, CRO or academic research.
• Practical knowledge of Good Clinical Practice and regulatory expectations for clinical data.
• Experience working with external vendors or Functional Service Providers and performing sponsor oversight.

Responsibilities

• Lead and oversee end‑to‑end data management for one or several clinical studies, ensuring quality, timelines and budget targets are met.
• Serve as the main contact for data management matters for internal teams and external vendors or CROs.
• Contribute to study planning and design with input to Data Management Plans, protocol‑related documents and study risk registers.
• Manage in‑stream data flow, cleaning, reconciliation and delivery of a clean study database and database lock.
• Oversee design and configuration of data capture tools (eCRF, eCOA) and integration with external data sources.
• Provide sponsor oversight of vendor performance, maintain TMF artifacts and support audits and inspections.

Skills

Clinical Data Management

Clinical Trial Designs

Data Management

Communication

Data Analysis

Data Standards

Teamwork

Risk Management

Education

Bachelor’s degree in a scientific, clinical, data or computer-related discipline

Tools

InForm

Rave

Veeva

eCOA

Job description

GSK in Poland is seeking an experienced professional to lead end-to-end clinical data management across multiple studies. You will drive data quality, timelines and regulatory compliance while coordinating with study teams and external partners.

You will oversee data capture tools (eCRF, eCOA) and data flow, ensuring clean databases and timely database locks. This role offers growth within a global biopharma environment and hybrid work arrangements in Poland.