Oncology Clinical Scientist - Data & Trends

Worldwide Clinical Trials; Portland (OR); 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, interpret, and assess oncology solid tumor data, communicating key findings to Clients and the study team. You will work with the Medical Monitor and contribute to high quality data, CSR preparation, and timely data review.

You will develop oncology data review plans, analyze efficacy and safety data, present trends, mentor junior staff, and collaborate with Data Management, Pharmacovigilance, and external

Qualifications

• Strong knowledge of oncology clinical development processes and study design.
• Proficiency with EDC systems and data visualization platforms.
• Excellent written, oral communication, and presentation skills.

Responsibilities

• Develop oncology clinical data review plans for assigned studies.
• Present key oncology data trends and findings 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.
• Utilize visual analytics tools to interpret and communicate data insights.

Skills

Oncology clinical data analysis

Regulatory understanding

EDC systems proficiency

Data visualization tools

Communication skills

Willingness to travel

Education

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

Tools

Microsoft Office

EDC systems

Data visualization platforms

Job description

Worldwide Clinical Trials in the United States is seeking a Clinical Scientist to review, interpret, and assess oncology solid tumor data, communicating key findings to Clients and the study team. You will work with the Medical Monitor and contribute to high quality data, CSR preparation, and timely data review.

You will develop oncology data review plans, analyze efficacy and safety data, present trends, mentor junior staff, and collaborate with Data Management, Pharmacovigilance, and external