KEY RESPONSIBILITIES:
* Advocate for increased knowledge within CfDA on new EU HTA regulation, its impact and implementation phases
* Ensure an effective collaboration between CfDA and HEOR throughout the product lifecycle and implement strategies to increase HTA knowledge and expertise within CfDA
* Provide consulting and hands-on support for CfDA team members undertaking analyses for HTA purposes
* Provide statistical expertise in causal inference, indirect comparison, PRO evaluation and subgroup analysis
* Development and maintenance of a range of resources for HTA purposes, including TFL shell and code library
* Interact with multifunctional internal stakeholders and Subject Matter Experts to deliver value by developing novel, practical, scientific data-driven solutions to meet HTA business needs
* Network with HTA Subject Matter Experts across industry
* Involvement in process development and maintenance of statistical activities related to HTA
REQUIREMENTS:
* Degree educated in Statistics/Biostatistics or related subject with high statistical content, coupled with post graduate statistical experience gained within biopharmaceutical industry or medical research
* Superior understanding of statistical principles, methods, applications and procedures, specifically related to the HTA setting
* Highly proficient in biostatistical software, including R and SAS
* Life cycle drug development experience
* Excellent analytical and problem-solving skills
* Experience working effectively in a globally dispersed team and with cross functional partners
* Excellent communication skills both oral and written
* Experience in developing policies and SOPs