AIXIAL GROUP

• Representing the CRO externally to current and prospective clients • Utilizing clinical and therapeutic expertise during pre-sales and sales engagements • Establishing trial strategies including cross departmental and vendor communications • Engaging with clients directly to gather intelligence regarding future projects • Providing leadership support to business development activities • Ensuring trial strategies align with compliance to relevant regulations

• Creation and QC of study specifications for SDTM datasets, and statistical programming and QC of SDTM datasets for Phase I-IV trials. • Creation and QC of study specifications for ADaM datasets, and statistical programming and QC of ADaM datasets for Phase I-IV trials. • Statistical programming and QC of tables, listings and figures for Phase I-IV trials. • Responsible for the quality and timeliness of assigned statistical deliverables. • As Lead Statistical Programmer, primarily responsible for all statistical programming activities on assigned studies including planning and coordination of activities for assigned statistical programming team members. • Active participation in improvements to departmental processes and procedures. • Provide mentoring within the Statistical Programming team.

• To provide expert statistical input to Phase I-IV global clinical trials, including the design of clinical trials (protocol, sample size, randomisation, etc) and the production and review of analysis and reporting deliverables (including statistical analysis plans) on behalf of and/or in conjunction with Aixial Group clients. • Creation and QC of study specifications for ADaM datasets, and statistical programming and QC of ADaM datasets for global Phase I-IV trials. • Statistical programming and QC of tables, listings and figures for global Phase I-IV trials. • Responsible for the quality and timeliness of statistical deliverables. • As lead Statistician, to be primarily responsible for all statistical activities on allocated studies including planning and coordination of activities for assigned statistical team members.

• Creation and QC of study specifications for SDTM datasets, and statistical programming and QC of SDTM datasets for Phase I-IV trials. • Creation and QC of study specifications for ADaM datasets, and statistical programming and QC of ADaM datasets for Phase I-IV trials. • Statistical programming and QC of tables, listings and figures for Phase I-IV trials. • Responsible for the quality and timeliness of assigned statistical deliverables. • As Lead Statistical Programmer, primarily responsible for all statistical programming activities on assigned studies including planning and coordination of activities for assigned statistical programming team members. • Active participation in improvements to departmental processes and procedures. • Provide mentoring within the Statistical Programming team.

• To provide expert statistical input to Phase I-IV global clinical trials, including the design of clinical trials (protocol, sample size, randomisation, etc) and the production and review of analysis and reporting deliverables (including statistical analysis plans) on behalf of and/or in conjunction with Aixial Group clients. • Creation and QC of study specifications for ADaM datasets, and statistical programming and QC of ADaM datasets for global Phase I-IV trials. • Statistical programming and QC of tables, listings and figures for global Phase I-IV trials. • Responsible for the quality and timeliness of statistical deliverables. • As lead Statistician, to be primarily responsible for all statistical activities on allocated studies including planning and coordination of activities for assigned statistical team members.

• Managing and executing on small to large, global, complex, full-service clinical project(s) or multi-project programs • Assessing and delivering on KPIs, including identifying project study trends, budgets, performance metrics and project reports • Providing support to project team members • Managing client expectations and ensuring client satisfaction

• Managing small to large, global, complex, full-service project(s) or multi-project programs. • Plan and execute multiple phase I-IV studies to agreed timelines, scope, and budget, managing all aspects including overseeing vendors, to ensure patient safety, data integrity, and adherence to contract and protocol.

• Representing the CRO externally to current and prospective clients • Utilizing clinical and therapeutic expertise during pre-sales and sales engagements • Establishing trial strategies which includes cross departmental and vendor communications • Engaging with clients directly to gather meaningful intelligence regarding future projects • Providing leadership support to business development activities such as participating in capabilities presentations and bid defence meetings • Overseeing programmes and projects within the Clinical and Regulatory Operations or Full Services project portfolio • Leading strategic planning and implementation of process improvement • Ensuring trial strategies align with compliance to relevant regulations and industry quality standards • Establishing and maintaining strong working relationships with clients, vendors and company staff