Oncology Clinical Scientist, Data & Insights Lead

Worldwide Clinical Trials; Jefferson City (MO); On-site; USD 79,000 - 157,000; Full time

Job summary

Worldwide Clinical Trials seeks a Clinical Scientist to review and interpret oncology solid tumor data, collaborating with Medical Monitors and clients to ensure high-quality data and CSR integrity. The role supports data review, statistical interpretation, and scientific writing across regulatory documents.

The candidate should have an advanced clinical degree with 8+ years of industry experience in oncology, strong data visualization skills, and proficiency with EDC systems.

Qualifications

• Advanced clinical degree preferred (e.g., PharmD, PhD, MSN, ARNP).
• 8+ years of industry-related experience in Oncology.
• Proficiency with EDC systems and data visualization.

Responsibilities

• Develop oncology clinical data review plans for assigned studies.
• Conduct ongoing oncology data review and analysis using listings, tables, figures, and graphs.
• Present key oncology data trends to Medical Monitor, Study Team, and Client.
• Collaborate with cross-functional teams to ensure accurate data reporting.
• Track and analyze potential safety events with Pharmacovigilance and Medical Monitoring.
• Create data summary slides for Safety Review 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 on protocol inquiries.
• Review regulatory documents and provide scientific writing support.

Skills

Oncology data analysis

Data visualization

GCP & ICH

Communication & presentation

Cross-functional collaboration

Independent work

Education

Advanced clinical degree (PharmD/PhD/MSN/ARNP)

Tools

EDC systems

Data visualization platforms

Job description

Worldwide Clinical Trials seeks a Clinical Scientist to review and interpret oncology solid tumor data, collaborating with Medical Monitors and clients to ensure high-quality data and CSR integrity. The role supports data review, statistical interpretation, and scientific writing across regulatory documents.

The candidate should have an advanced clinical degree with 8+ years of industry experience in oncology, strong data visualization skills, and proficiency with EDC systems.