Clinical Scientist - Oncology - US - Remote
Worldwide Clinical Trials · Durham, NC
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
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.
What they're looking for
- 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
What you'll be doing
- 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
Key requirements
- Therapeutic area
- Oncology
Privacy & handoff
This role links to Worldwide Clinical Trials's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.