Biostatistician - Global Biostatistics

Home-Based/Hybrid: UK/EMEA/South Africa

The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability.

We have one of the largest Biostatistics departments within the industry of around 1,100+ staff, to which we engage the full range of industry-leading resources and expertise spanning all study phases and therapeutic areas.

Due to continued growth, we are seeking new brave minds to join our award winning and innovative department. You will work globally and across all therapeutic areas as IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.

THE ROLE

You will provide statistical consulting and technical support as it relates to the design, statistical analysis, and regulatory submissions of clinical trial studies. 

Collaborating with medical and programming staff to produce interim reports and final reports, allowing a comprehensive understanding and interpretation of the clinical trial data and outcome. 

Biostatistician Overview:

• Perform protocol development, sample size calculation, protocol and CRF review, and advise data management on database design and critical data

• Coordinate the development of analysis plans, table shells, and programming specifications

• Understand scope of work, budget, and quote assumptions, estimate the work completed, manage scope, and provide revenue and resource forecasts for single studies

• Consult on operational/statistical/therapeutic area topics

• Prepare proposal text and attend bid defense meetings

• Communicate with clients regarding study protocol

• Act as statistical team lead for single complex studies or groups of studies

• Primary point of contact for the study team - communicate with team members regarding execution as it relates to timelines, budget, data quality, and interpretation of results

• Provide expert statistical input and review of deliverables for validation requirements

• Review of the clinical study report to ensure statistical integrity in the reporting of the results

• Interpret analysis and craft statistical sections of integrated reports

• Provide training and mentoring to team members and department staff

You can help us bring clinical trial statistical analysis into the next generation.  Award winning and innovative; we will give you access to cutting-edge in-house technology, allowing you to work on global projects across a variety of therapeutic areas. 

Be challenged in a fast-paced team environment that is collaborative in performing biostatistical analyses and statistical programming. 

Development opportunities and mentoring at all levels enable you to progress your long-term career in the direction you choose.

THE PERSON

We know that meaningful results require not only the right approach, but also the right people.

You should possess a MSc or PhD in Biostatistics or Statistics, with relevant experience. 

• Work experience in statistics

• Ability to communicate and explain statistics

• Exhibit routine and complex analytical skills 

• A focus on quality and accuracy

• A good understanding of Good Clinical Practice and ICH guidelines

• Experience in programming in SAS

• Ability to independently lead

• Take initiative and work with integrity

• Ability to establish and maintain effective working relationships

JOIN US:

From camaraderie to professional development, working at IQVIA provides unique opportunities to advance your career alongside a group of diverse and talented colleagues.

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.

Whatever your career goals, we are here to ensure you get there!