Oncology Clinical Scientist - Data Insights Lead

Worldwide Clinical Trials; United States; Remote; USD 79.000 - 157.000; Vollzeit

Zusammenfassung

Worldwide Clinical Trials is seeking a Clinical Scientist to review, interpret, and assess oncology clinical data, with a focus on solid tumor data, and communicate key findings to Clients and study teams.

The role partners with Medical Monitors, data management, and cross‑functional teams to ensure data integrity, CSR quality, and timely regulatory submissions, while mentoring junior staff and traveling as needed.

Qualifikationen

• Requires advanced clinical or scientific degree with 8+ years oncology experience.
• Proficient with EDC systems and data visualization tools.
• Strong knowledge of oncology development processes and study design.
• Excellent written and verbal communication, collaboration, and presentation skills.
• Willingness to travel as needed.

Aufgaben

• Develop oncology clinical data review plans for assigned studies.
• Conduct ongoing oncology data review and analysis using listings, tables, figures, graphs, and EDC.
• Present oncology data trends to the Medical Monitor, Study Team, and Client.
• Collaborate with cross-functional study team members to ensure protocol-defined variables are collected and reported accurately.
• Track and analyze potential safety events in collaboration with Pharmacovigilance and Medical Monitoring.
• Create data summary slides for Safety Review Committee Meetings.
• Query data on EDC during clinical review with timely follow up.
• Partner with vendors and study team to ensure accurate endpoint reporting.
• Mentor and train junior staff.
• Utilize visual analytics tools to interpret data insights.

Kenntnisse

Oncology data analysis

EDC systems

Data visualization

Microsoft Office

Ausbildung

Advanced clinical or scientific degree

Tools

EDC software

Data visualization platforms

Jobbeschreibung

Worldwide Clinical Trials is seeking a Clinical Scientist to review, interpret, and assess oncology clinical data, with a focus on solid tumor data, and communicate key findings to Clients and study teams.

The role partners with Medical Monitors, data management, and cross‑functional teams to ensure data integrity, CSR quality, and timely regulatory submissions, while mentoring junior staff and traveling as needed.