Oncology Clinical Scientist - Data Insights for Trials

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

Job summary

Worldwide Clinical Trials is seeking a Clinical Scientist to review, interpret, and assess oncology solid tumor data, communicating findings to Clients and study teams. Collaborate with Medical Monitor to ensure high-quality data and integrity of CSR and regulatory documents.

You will work with cross-functional teams to meet timelines, mentor junior staff, and contribute to data-driven study strategy discussions. Willingness to travel and strong communication are required.

Qualifications

• Advanced oncology clinical development knowledge and study design principles.
• Experience with solid and liquid tumor data review.
• Clinical data analysis and interpretation with regulatory awareness.

Responsibilities

• Develop oncology data review plans for assigned studies.
• Conduct ongoing oncology data review and analysis using listings, tables, figures, and graphs.
• Present key oncology trends to Medical Monitor, Study Team, and Client.
• Collaborate with cross-functional teams to ensure accurate reporting of protocol-defined variables.
• Track and analyze potential safety events with Pharmacovigilance and Medical Monitoring.
• Create data summary slides for Safety Review Committee and Data Review Meetings.
• Query data on EDC during clinical review with timely follow-up.
• Partner with vendors to ensure accurate endpoint reporting.
• Serve as contact for site staff and monitors regarding protocol and inquiries.
• Collaborate with Data Management on CRF design and data quality plans.
• Review data-driven sections of CSRs, INDs, NDAs/BLAs, etc.
• Provide scientific writing support (patient narratives, abstracts, posters, presentations).
• Mentor and train junior staff.
• Utilize visual analytics tools to interpret data insights.

Skills

Oncology data analysis

Clinical data interpretation

Oral and written communication

Presentation skills

Travel willingness

Education

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

Tools

EDC systems

Data visualization platforms

Microsoft Office Suite

Job description

Worldwide Clinical Trials is seeking a Clinical Scientist to review, interpret, and assess oncology solid tumor data, communicating findings to Clients and study teams. Collaborate with Medical Monitor to ensure high-quality data and integrity of CSR and regulatory documents.

You will work with cross-functional teams to meet timelines, mentor junior staff, and contribute to data-driven study strategy discussions. Willingness to travel and strong communication are required.