Oncology Clinical Scientist - Data Insights Lead

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

Job summary

Worldwide Clinical Trials is a global midsize CRO focused on oncology data review and high‑quality clinical data integrity. The Clinical Scientist reviews solid tumor data, presents trends to clients, and collaborates with Medical Monitor and study teams to ensure accurate reporting.

The role requires advanced oncology knowledge, robust data analysis skills, and the ability to mentor junior staff while contributing to regulatory documentation and scientific writing. Travel as needed.

Qualifications

• Advanced clinical or scientific degree preferred (e.g., PharmD, PhD, MSN, ARNP) with 8+ years of industry‑related experience in Oncology.
• Proficiency in Microsoft Office Suite.

Responsibilities

• Develop oncology clinical data review plans for assigned studies.
• Present key 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.
• Mentor and train junior staff.
• Provide scientific writing support, including patient narratives, abstracts, posters, and presentations.

Skills

Oncology clinical data analysis

Data visualization tools

GCP & ICH guidelines

Regulatory documentation

MS Office proficiency

Education

Advanced clinical or scientific degree (e.g., PharmD, PhD, MSN, ARNP)

Tools

EDC systems

Data visualization platforms

Job description

Worldwide Clinical Trials is a global midsize CRO focused on oncology data review and high‑quality clinical data integrity. The Clinical Scientist reviews solid tumor data, presents trends to clients, and collaborates with Medical Monitor and study teams to ensure accurate reporting.

The role requires advanced oncology knowledge, robust data analysis skills, and the ability to mentor junior staff while contributing to regulatory documentation and scientific writing. Travel as needed.