• Support decision-making in clinical design, submission and interpretation by identifying, benchmarking, extracting and presenting back meaningful facts and data via internal and external competitive intelligence information sources
• Using techniques such as text mining and data visualization, extracting key relevant information, enabling timely and objective clinical study design decision
• Maintain a repository of key data, bringing together key historical decisions for the wider team to use and refer to
• Plan and work independently and take responsibility for specific deliveries within a drug project, and ensure a high level of quality is built into deliverables

• M.Sc. or PhD
• Experience in conducting literature and database searches
• Understanding/Exposure of the pharmaceutical drug development process (setting could include, but are not limited to: Clin Ops, Regulatory, Early development, Medical Affairs, Competitive/Regulatory Intelligence)
• Experience working in oncology data within the pharmaceutical industry
• Experience in the application of information and knowledge management in a clinical or scientific setting
• Good written and verbal communication skills including presentation skills and proficiency in communicating complex information to a diverse audience
• Good organizational skills with the ability to multitask, set priorities and follow a timeline
• Great attention to detail

What you need to do now

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