Lead Clinical Data Manager – Oncology (Poland, CRO)

GRUPA NEUCA; Polska; Hybrid; PLN 180,000 - 260,000; Full time

Benefits offered by this job

Free legal advice

Employee referral program

Day off on birthday

Emergency support fund

Veterinary package for dogs and cats

Job summary

GRUPA NEUCA seeks a Lead Data Manager to oversee allocated projects, ensuring all data management deliverables align with timelines and quality standards. You will guide the DM team, allocate resources, and coordinate with Project Managers to meet contracted milestones.

Responsibilities include ensuring compliance with GCP and SOPs, performing comprehensive data quality checks, and reconciling clinical, safety, and laboratory data using appropriate systems.

Qualifications

• University degree (bioengineering, life science or related subject preferred) from an accredited institution.
• Fluency in English.
• Minimum 2 years of experience in effective clinical data management practices.
• Excellent knowledge of MS Excel.

Responsibilities

• Lead Data Manager for allocated projects and ensure DM deliverables meet established timelines.
• Provide instruction to the DM study team and review outputs, adjusting as needed.
• Manage resource allocations within the project and coordinate with leads across disciplines.
• Oversee compliance with GCP, SOPs, and study protocols; ensure data quality and integrity.
• Build timelines with the Project Manager to meet milestones and communicate with project team.
• Support risk mitigation by staying aware of other Biometrics deliverables.
• Perform quality control across all study aspects.
• Reconcile clinical, safety, and laboratory data; utilize local lab systems for data loads.

Skills

Clinical data management

Analytical thinking

Independent planning

Client communication

Teamwork

Education

Bioengineering / Life Science degree

Tools

MS Excel

R

SAS

Job description

GRUPA NEUCA seeks a Lead Data Manager to oversee allocated projects, ensuring all data management deliverables align with timelines and quality standards. You will guide the DM team, allocate resources, and coordinate with Project Managers to meet contracted milestones.

Responsibilities include ensuring compliance with GCP and SOPs, performing comprehensive data quality checks, and reconciling clinical, safety, and laboratory data using appropriate systems.