Senior Statistician - Italy - P

12 May 2021
10 Jun 2021
Full Time
Contract Type
Experience Level
Experienced (non-manager)
Job Title: Senior or Principal Statistician

Location: Milan, Italy

Schedule: Full-time, Office Based with Home Based Flexibility

Are you an experienced statistician looking for a company which can offer you real work-life balance? Are you interested in sharing your skills and expertise in a growing CRO, where you can influence key decisions and truly make an impact? CROMSOURCE is continuing to expand our Biometrics team at our office in Milan (with some home based flexibility) and we want the perfect Senior or Principal Statistician to help influence this growth.

We are looking for an experienced statistician to support our growing team of statisticians and programmers. You will work on varied therapeutic areas, providing analysis and expertise and as a key study team member you will have direct contact with our clients. There will also be opportunities to support the Management Team in organising and executing the departmental process initiatives and may also be the opportunity to act as the Project Lead Statistician on groups of customer studies.

What CROMSOURCE can offer you:
  • True work-life balance with flexible working hours
  • Close management support to ensure workload is managed within a normal working week
  • Opportunities for career progression/development, enabling you to progress within the department
  • Variety within your work - our clients are small and mid-sized pharmaceutical, biotechnology and medical device companies; you can become truly embedded within the pharmaceutical aspect, including having direct contact with bodies such as the FDA and EMA
  • The chance to work not only on clinical, IMP studies, but also medical device projects too

Main Job Tasks and Responsibilities
  • Leads the statistical analysis of a clinical study in compliance with the analysis plan and protocol
  • Provides high quality statistical support direct to our clients whilst managing projects
  • Provides statistical and methodological input for sample size calculation and protocol development
  • Develops a detailed statistical analysis plan and related mock shells
  • Performs quality control and senior review of the tables, listings, figures, datasets, inferential analysis and statistical text
  • Leads Data Review Meetings
  • Writes statistical reports and/or sections for the integrated study report, reviews the draft study report, and ensures that all data presented is correct
  • Responsible for project scope, efficiencies, milestones and budgets and completing work according to CROMSOURCE SOPs
  • Expert person, central reviewer of ADaM datasets, deliverables and processes, keeping abreast with all regulatory developments within CDISC
  • Contribute to the development, implementation and maintenance of the quality system and suggests process improvements
  • Assists in providing input into RFPs and bid defense meetings

Education and Experience
  • Advanced Degree in sciences, with substantial statistics component
  • At least eight years of experience as a statistician in life science/pharmaceutical/CRO environment
  • Proven organizational and problem solving/decision making skills
  • Expert knowledge of the applicable regulatory guidance
  • Proficient in SAS software
  • Proficient in Microsoft Office (e.g. Word, Excel, Outlook)
  • Fluent in English and local language(s)
  • Good communication skills
  • Advantageous, project management and leadership skills

The Application Process:

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. If you would like to discuss the role before applying through the website @, please contact for more information.


CROMSOURCE is an independent, international Contract Research Organisation (CRO) operating in over 40 Countries and 16 offices with approximately 500 professional team members, making it one of the largest independent CROs in Europe. Our international headquarters located in Verona, Italy and Waltham, USA and with local offices in Belgium, The Netherlands, Germany, Poland, Russia, Spain, Switzerland and the United Kingdom.

By joining our client teams, you can be part of making a difference in the lives of people and experience a fulfilling and rewarding career. Together, we help our clients succeed in their work developing medicines and medical devices for patients around the world.

Keywords Statistician Biostatistician Senior Statistician Senior Biostatistician Principal Statistician Statistical Scientist Statistical Analysis Line Management Milan Italy Veneto Italia CRO Medical Devices Clinical Research Organisation
Skills: Biostatistician Location: Italy Share:

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