Oncology Clinical Scientist — Data-Driven Trial Expert

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

Job summary

Worldwide Clinical Trials in the United States is seeking a Clinical Scientist to review and interpret oncology solid tumor data, communicating trends to Clients and study teams while upholding data integrity and CSR quality.

You will develop data review plans, analyze efficacy and safety data, present findings to Medical Monitor and Client, and mentor junior staff. Advanced degree and 8+ years preferred; travel may be required.

Qualifications

• Advanced clinical degree with 8+ years of oncology industry experience.
• Strong knowledge of oncology development, study design and safety concepts.
• Proficiency with EDC systems and data visualization platforms.

Responsibilities

• Develop oncology clinical data review plans for assigned studies.
• Perform ongoing oncology data review and analysis including efficacy and safety data.
• Present trends to Medical Monitor, Study Team and Client.
• Collaborate to ensure accurate data collection and reporting.
• Provide scientific writing support and mentor junior staff.

Skills

Oncology data analysis

EDC systems

Data visualization

GCP & regulatory

Written & oral communication

Education

Advanced clinical/scientific degree + 8+ years experience

Tools

EDC systems

Data visualization platforms

MS Office

Job description

Worldwide Clinical Trials in the United States is seeking a Clinical Scientist to review and interpret oncology solid tumor data, communicating trends to Clients and study teams while upholding data integrity and CSR quality.

You will develop data review plans, analyze efficacy and safety data, present findings to Medical Monitor and Client, and mentor junior staff. Advanced degree and 8+ years preferred; travel may be required.