Senior Oncology Clinical Scientist - Data-Driven Trials

Worldwide Clinical Trials; Georgia; On-site; USD 79,000 - 157,000; Full time

Job summary

Worldwide Clinical Trials in the United States seeks a Clinical Scientist to lead oncology data review and interpretation of solid tumor datasets, ensure high-quality CSR content, and communicate trends to clients and study teams.

You will collaborate with Medical Monitor, Data Management, and vendors to support study timelines, perform data visualization, and contribute scientific writing for abstracts and posters.

Qualifications

• Advanced oncology clinical data analysis and interpretation experience.
• Experience with solid and liquid tumor data review and imaging data review.

Responsibilities

• Develop oncology clinical data review plans for assigned studies.
• Conduct ongoing oncology clinical data review and analysis using EDC listings, tables, figures, and visual analytics.
• Present key oncology data trends to the Medical Monitor, Study Team, and Client.
• Collaborate with cross-functional teams to ensure data quality and protocol-defined variables.
• Track and analyze potential safety events with Pharmacovigilance and Medical Monitoring.
• Create data summary slides for Safety Review Committee meetings and Data Review Meetings.
• Query data on EDC data during clinical review and identify protocol deviations.
• Partner with vendors to ensure accurate endpoint reporting.
• Serve as a point of contact for site staff and monitors for inquiries.
• Provide scientific writing support for narratives, abstracts, posters, and presentations.
• Mentor and train junior staff.
• Utilize visual analytics to interpret data insights.

Skills

Oncology data analysis

GCP/ICH knowledge

Communication skills

Team collaboration

Travel readiness

Education

Advanced clinical degree

Tools

Microsoft Office

EDC systems

Data visualization tools

Job description

Worldwide Clinical Trials in the United States seeks a Clinical Scientist to lead oncology data review and interpretation of solid tumor datasets, ensure high-quality CSR content, and communicate trends to clients and study teams.

You will collaborate with Medical Monitor, Data Management, and vendors to support study timelines, perform data visualization, and contribute scientific writing for abstracts and posters.