Global Immunology Clinical Science Lead

Biopharma Careers; Warszawa; On-site; PLN 328,000 - 398,000; Full time

Job summary

Bristol Myers Squibb in Warsaw, Poland, is seeking a Senior Manager, Global Clinical Science - Immunology, to design and execute assigned clinical trial activities and work closely with the clinical team to ensure successful conduct of trials.

The role may serve as Clinical Trial Lead for one or more trials and requires collaboration with cross-functional study teams, maintaining high data quality and regulatory readiness.

Qualifications

• Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field) is preferred.
• Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations.
• Ability to understand assigned protocol(s) and their requirements.
• Basic planning/project management skills.
• Detail-oriented with commitment to quality.

Responsibilities

• Collaborate with external partners (e.g., KOLs) and provide regular updates to management.
• Develop Protocol and ICF documents/amendments and present to governance committees.
• Conduct literature review and submit clinical documents to TMF.
• Develop training materials for sites and CRAs and present at SIVs and Investigator meetings.
• Review clinical narratives and monitor data for trends.
• Develop Data Review Plan with Data Management.
• Ensure CRF design supports data collection per protocol.

Skills

GCP/ICH knowledge

Study design

Statistics

Data review

Critical thinking

Problem solving

Communication

Microsoft Word

Microsoft Excel

PowerPoint

Education

Life sciences degree

Tools

Pt Profiles

Reporting tools

Job description

Bristol Myers Squibb in Warsaw, Poland, is seeking a Senior Manager, Global Clinical Science - Immunology, to design and execute assigned clinical trial activities and work closely with the clinical team to ensure successful conduct of trials.

The role may serve as Clinical Trial Lead for one or more trials and requires collaboration with cross-functional study teams, maintaining high data quality and regulatory readiness.