Senior Oncology Clinical Scientist

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

Benefits offered by this job

Competitive benefits package

Transparent compensation

Pay equity and transparency

Job summary

Worldwide Clinical Trials is seeking a Clinical Scientist to review and interpret oncology clinical data, focusing on solid tumor data, and to communicate findings to clients and study teams. You will work with the Medical Monitor and cross-functional groups to ensure high-quality data and timely CSR preparation.

The role emphasizes data analysis, scientific writing, and collaboration across departments with opportunities for mentorship and travel as needed.

Qualifications

• Strong knowledge of oncology clinical development processes and study design principles.
• Deep understanding of oncology product profiles and safety concepts.
• Experience with solid and liquid tumors, imaging data review.
• Clinical understanding of the physiological effects of oncology therapies on organ systems.
• Proficient with EDC systems and data visualization.

Responsibilities

• Develop oncology clinical data review plans for assigned studies.
• Conduct ongoing oncology clinical data review and analysis using listings, tables, figures, graphs, and EDC.
• 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.
• Contribute to discussions on potential study or strategy modifications based on clinical data review.
• Create data summary slides for Safety Review Committee Meetings, Data Review Meetings with support from Director.
• Query data on EDC during Clinical review with timely follow-up.
• Partner with vendors and study team members to ensure accurate endpoint reporting.
• Serve as a point of contact for site staff and monitors for protocol and clinical inquiries.
• Collaborate with Data Management on CRF design, CRF instructions, and data quality plans.
• Review data-driven sections of regulatory and clinical reporting documents.
• Provide scientific writing support, including patient narratives, abstracts, posters, and presentations.
• Mentor and train junior staff.
• Utilize visual analytics tools to interpret and communicate data insights.
• The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

Skills

Oncology clinical development

Data analysis

Scientific writing

Communication skills

Regulatory knowledge

Travel willingness

Education

Advanced clinical degree (PharmD/PhD/MSN/ARNP)

Tools

EDC systems

Microsoft Office Suite

Data visualization platforms

Job description

Worldwide Clinical Trials is seeking a Clinical Scientist to review and interpret oncology clinical data, focusing on solid tumor data, and to communicate findings to clients and study teams. You will work with the Medical Monitor and cross-functional groups to ensure high-quality data and timely CSR preparation.

The role emphasizes data analysis, scientific writing, and collaboration across departments with opportunities for mentorship and travel as needed.