Senior Oncology Clinical Scientist – Data Insights

Worldwide Clinical Trials Holdings, Inc.; Georgia; Hybrid; USD 79,000 - 157,000; Full time

Job summary

Worldwide Clinical Trials Holdings, Inc. is seeking a Clinical Scientist in Oncology to lead the review and interpretation of solid tumor data and present findings to clients and study teams.

You will partner with the Medical Monitor and cross‑functional colleagues to ensure data integrity and regulatory readiness. The role requires an advanced clinical or scientific degree with 8+ years in oncology, strong data interpretation skills, and experience with EDC systems and data visualization.

Qualifications

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

Responsibilities

• Develop oncology clinical data review plans for assigned studies.
• Conduct ongoing oncology clinical data review and analysis of clinical data (efficacy, safety) using listings, tables, figures and graphs.
• 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 with Pharmacovigilance and Medical Monitoring.
• Create data summary slides for Safety Review Committee and Data Review Meetings.

Skills

Oncology clinical development

Data analysis

EDC systems

GCP/ICH knowledge

Communication & presentations

Cross-functional collaboration

Travel willingness

Scientific writing

Education

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

Tools

EDC systems

Data visualization tools

Microsoft Office Suite

Job description

Worldwide Clinical Trials Holdings, Inc. is seeking a Clinical Scientist in Oncology to lead the review and interpretation of solid tumor data and present findings to clients and study teams.

You will partner with the Medical Monitor and cross‑functional colleagues to ensure data integrity and regulatory readiness. The role requires an advanced clinical or scientific degree with 8+ years in oncology, strong data interpretation skills, and experience with EDC systems and data visualization.