How would you like to join a new team to expand their global oncology Statistician group in this leading Pharmaceutical company working with colleagues in Asia, Europe and the USA? This group has high visibility within the organisation giving your better access with senior stakeholders to make a key difference in the company.
This is a fantastic opportunity for an experienced Statistician who would like to work across all phases from early to late phases within Oncology trials joining a global team of experienced Clinical Statisticians.
Objectives of the role:
*Collaborates with representatives from other functions to plan, execute, analyse and report
*relevant studies in the role of a study statistician for oncology clinical development studies
*Contributes to the preparation of the study protocols
*Develops the statistical analysis plan for the study as appropriate, and is involved in reporting results in the clinical study report.
*Facilitates and coordination of statistical activities for specific studies
*Assumes responsibility for the production and accuracy of the statistical deliverables and Interpretation of the results
A typical day will be project-level work:
*Project and study team meetings with clinicians, regulatory, market access
*Meetings to check with internal study statisticians, clinical data managers, clinical Programmers
*Study design work to be completed when the study is set up and regulatory-related activities
*Fortnightly one to one with managers to support and check-ins
*You'll be an experienced Statistician ideally with experience of Clinical Development within a Pharma or CRO environment.
*PhD or MSc in Biostatistics, Mathematics Statistics or, or similar related field
*You'll have experience of statistical programming languages of either SAS and R
*You'll have the keen interest to learn about Survival analysis
*You'll have excellent communication skills, like working in a team environment and be able to show the softer skills needed to work in a collaborative environment
You'll get to work at any phases of trials as well as different levels of responsibilities which you may not have access to in your current role. You won't be expected to work during the evenings or weekends, your well-being is of high importance and the balance with your family life. You'll have support from your manager but won't be micro-managed, you'll be given guidance but be able to manage your own time to deliver the project outcomes
This is either a remote role, office based or hybrid mix to suits your own personal needs.
If you're thinking about your next challenge and want to join a company that passionately cares about their employees and the work they are doing, get in touch today to discuss for an informal discussion.
Salary:Negotiable plus beneifts
Job published:3 months ago