Oncology Clinical Scientist: Data-Driven Trial Expert

Worldwide Clinical Trials; Virginia (MN); On-site; USD 79,000 - 157,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Scientist to oversee oncology data review and interpretation for solid tumor studies. You will collaborate with the Study Team and Clients to ensure high-quality data and timely CSR delivery.

The role requires an advanced clinical or scientific degree and 8+ years in oncology, with expertise in EDC and data visualization. Travel may be required as part of project delivery and client interactions.

Qualifications

• Advanced clinical or scientific degree preferred with 8+ years in Oncology.
• Proficiency in Microsoft Office Suite.
• Experience with EDC systems and data visualization platforms.

Responsibilities

• Develop oncology clinical data review plans for assigned studies.
• Conduct ongoing oncology data review and analysis using listings, tables and graphs.
• Present key oncology data trends to the Medical Monitor, Study Team, and Client.
• Collaborate with cross-functional teams to ensure accurate reporting.
• Track safety events with Pharmacovigilance and Medical Monitoring.
• Create data summary slides for review meetings.

Skills

Oncology clinical development

Data visualization

GCP/ICH knowledge

EDC systems

Education

Advanced clinical degree

Tools

EDC systems

Microsoft Office

Data visualization platforms

Job description

Worldwide Clinical Trials is seeking a Clinical Scientist to oversee oncology data review and interpretation for solid tumor studies. You will collaborate with the Study Team and Clients to ensure high-quality data and timely CSR delivery.

The role requires an advanced clinical or scientific degree and 8+ years in oncology, with expertise in EDC and data visualization. Travel may be required as part of project delivery and client interactions.