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
Contact Detail:
Blackfield Associates Recruiting Team