Clinical Scientist - Oncology - US - Remote

Worldwide Clinical Trials

Worldwide Clinical Trials seeks a Clinical Scientist to lead clinical data review and assessment for oncology trials. The role involves interpreting complex trial data, communicating insights to stakeholders, and supporting regulatory deliverables while working across cross-functional teams.

Responsibilities

Partner with cross-functional teams to develop and execute data review plans for accurate endpoint collection
Review and interpret clinical efficacy and safety data, identifying trends and generating actionable insights
Monitor safety events across studies, supporting risk identification and escalation decisions
Communicate clinical findings and recommendations to internal teams, leadership, and clients
Support development of clinical study reports, regulatory documents, and data summaries for review boards

Requirements

Advanced degree in clinical or science field (PharmD, PhD, MSN, MPH, or equivalent)
8+ years oncology clinical trial research experience with data review and interpretation
Proficiency with EDC systems, data visualization tools, and Microsoft Office applications
Strong knowledge of clinical development, study design, and GCP/ICH regulatory requirements
Excellent communication and presentation skills for diverse audiences
Strong analytical, organizational, and problem-solving abilities
Collaborative team player with attention to detail and independent judgment

Apply

Vacancy posted 5 days ago

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