Clinical Data Management Lead — End-to-End Trials

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

Benefits offered by this job

Hybrid work model

Job summary

GSK in Poland is seeking an experienced clinical data manager to lead end-to-end data management across studies, ensuring quality, timelines and regulatory compliance in a global context.

You will collaborate with study teams, vendors and CROs, oversee data capture tools (eCRF/eCOA), and support audits while contributing to study design and data standards, enabling reliable analyses and decisions in patient care. This role offers growth within a collaborative, patient-focused environment.

Qualifications

• Bachelor's degree in a scientific, clinical, data or computer-related discipline.
• Minimum of 4 years of experience in clinical data management or clinical trials in pharma, CRO or academic research.
• Experience with Good Clinical Practice and regulatory expectations for clinical data.

Responsibilities

• Lead end-to-end data management for one or several clinical studies, ensuring quality, timelines and budget targets.
• 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 and study risk registers.
• Manage data flow, cleaning, reconciliation and delivery of a clean study database with database lock.
• Oversee design and configuration of data capture tools (eCRF, eCOA) and integration with external data sources.

Skills

Agile thinking

Clinical data management

Clinical development

Data analysis

Data management

Communication

Teamwork

Education

Bachelor's degree in scientific/clinical/computer discipline

Job description

GSK in Poland is seeking an experienced clinical data manager to lead end-to-end data management across studies, ensuring quality, timelines and regulatory compliance in a global context.

You will collaborate with study teams, vendors and CROs, oversee data capture tools (eCRF/eCOA), and support audits while contributing to study design and data standards, enabling reliable analyses and decisions in patient care. This role offers growth within a collaborative, patient-focused environment.