Remote Senior Clinical Data Manager – Lead Sponsor Projects

Fortrea; Warszawa; On-site; PLN 180,000 - 300,000; Full time

Benefits offered by this job

Pension contributions

Health insurance

Remote working allowance

Job summary

Fortrea is seeking a Senior Clinical Data Manager to join our sponsor-dedicated CDM team from a home-based role in Poland. You will provide CDM leadership across assigned studies, manage vendor relationships, and ensure compliant delivery of data management deliverables on time.

You will lead multi-site studies, mentor junior staff, and collaborate with CRO partners and internal teams to maintain study standards, integrity, and high-quality data throughout the trial lifecycle.

Qualifications

• 8 years of combined early or late-stage DM experience with minimum 2 years of direct sponsor management and at least 2 years of mentoring experience.
• Extensive experience in clinical data management and leading studies in a CRO/Pharma setting.
• Understanding of RECIST criteria.
• Excellent oral and written communication and presentation skills.

Responsibilities

• Provide CDM leadership for one or more assigned projects or indications.
• Lead studies with healthy volunteer and patient populations, multi-site, complex protocol design, strong client management.
• Oversee vendor contracts, resourcing and budgets; monitor vendor performance.
• Ensure compliance with study model procedures and industry standards; manage risks and issues in CDM.

Skills

CDM leadership

Sponsor management

Mentoring

Clinical data management

Communication skills

Vendor management

Education

Life science degree

Tools

CDASH

SDTM

Clinical data systems

Job description

Fortrea is seeking a Senior Clinical Data Manager to join our sponsor-dedicated CDM team from a home-based role in Poland. You will provide CDM leadership across assigned studies, manage vendor relationships, and ensure compliant delivery of data management deliverables on time.

You will lead multi-site studies, mentor junior staff, and collaborate with CRO partners and internal teams to maintain study standards, integrity, and high-quality data throughout the trial lifecycle.