Senior Biostatistician
At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible - as a Senior Biostatistician you will join of the largest, award winning and innovative Biostatistics departments within the industry, around 1,100+ staff and bring clinical trial statistical analysis into the next generation.
You will be given access to cutting-edge in-house technology, allowing you to work on global projects across a variety of therapeutic areas including oncology and thanks to our development opportunities and mentoring at all levels you will be able to progress your long-term career in the direction you choose.
Key responsibilities:
* Building and maintaining effective customer relationships, driving statistical discussions, providing support and /or guidance for statistical activities.
* Acting as a statistical team lead role on single studies. Working closely with the Project Team Lead and supervisor to deliver on time, with high quality and within budget.
* Running meetings, documenting where necessary and following up on actions. Actively participates in internal project team meetings, provides timely progress updates. As a lead, you will have input on estimate at completion (EAC) reporting.
* Writing Statistical Analysis Plan (SAP) and Shells including performing quality control review (QC) of SAPs and shells.
* Writing and maintaining programming specifications. Programs assigned datasets to industry standards. Handles dataset derivations and assignment.
* Training and mentoring staff regarding operational items. Supporting colleagues and providing motivation as needed.
* Identifying risks to project delivery and/or quality and spends time to proactively avoid as well as proposes solutions to mitigate risks. Where possible, anticipate risks to minimize need for study level escalations.
* Assisting with protocol development, sample size calculation, protocol, and case report form (CRF) review.
* Performing quality control (QC) review of the statistical section of a protocol (making best possible use of resources and expertise within the organization (e.g. Libraries, templates, and consultants for complex statistical methods).
Key requirements:
* BSc or MSc degree Biostatistics or related field and 4-6 years relevant experience within the life science industry
* Familiarity with moderately complex statistical methods that apply to applicable clinical trials.
* Strong working knowledge of SAS computing package and CDISC SDTM and ADaM, CRO background
* Ability to effectively manage multiple tasks and projects.
What is in it for you?
* Interesting and innovative projects
* Collaborative and inspirational working environment / atmosphere
* Excellent career development and progression opportunities
* Competitive salary
We know that meaningful results require not only the right approach, but also the right people. Embrace your curiosity and grow your career in an exciting environment where development is a priority. Think boldly and disrupt conventional thinking.
Enjoy what you do.
Kind regards,
Anetta Kotynska
Senior Talent Acquisition Specialist
Talent Acquisition, Data Sciences, Safety & Regulatory (DSSR)
DL: +44(0)118 450 1883
M: +44(0)7367 699299
