Clinical Scientist
About the role
The Clinical Scientist is responsible for the review, interpretation, and assessment of oncology clinical data specifically solid tumor data with key findings communicated to Clients and study team. The Clinical Scientist works closely with the Medical Monitor as appropriate. This role communicates and presents clinical trends and findings to the Study Team and Clients while working collaboratively to ensure high quality data, maintain the highest integrity of the clinical database and clinical study reports (e.g., CSR). The Clinical Scientist partners with Clients, subcontractors, and internal study team members to meet project timelines and expectations related to clinical data review.
We love knowing that someone is going to have a better life because of the work we do.
Responsibilities
- Develop oncology clinical data review plans for assigned studies.
- Conduct ongoing oncology clinical data review and analysis of clinical data, (e.g., efficacy, safety related data components) utilizing listings, visual analytics, tables, figures, graphs, and EDC continually
- 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