About the role

Senior Statistician

Plus-Project are excited to announce that we currently have openings for experienced Senior Statisticians based in the UK. All opportunities are under the FSP model; hence you must feel comfortable working in this environment & ideally have prior experience. The ability to perform a lead study statistician role is essential; study design or Bayesian experience is desirable.

Key Responsibilities:

• Act as lead statistician for multiple projects with any level of complexity.
• Collaborate in the process of protocol development by choosing an appropriate study design, including statistical methodologies, calculating necessary sample size to achieve a pre-specified power, and writing the statistical section of the protocol.
• Collaborate cross-functionally with study teams members to effectively deliver high quality results.
• Perform statistical review of relevant study documentation (i.e. case report form, randomisation specification, dataset specifications) and clinical study reports.
• Author and review Statistical Analysis Plans (SAPs) based on the protocol, including development of output shells for tables, figures and listings.
• Programming and QC of efficacy analysis datasets and associated tables, figures and listings.
• Participate in Data Safety Monitoring Board and/or Data Monitoring Committee activities, including charter development.
• Prepare key portions of the integrated clinical/statistical report, ISS and ISE, including sections related to data handling and statistical methodology, patient accountability, baseline compatibility, and efficacy results.

Your Profile

• Master's Degree or PhD in Statistics (or related discipline)
• At least 4 years of experience working as a Statistician in clinical drug development
• Excellent oral and written communication skills
• Excellent analytical skills
• Proficiency in SAS / R programming languages
• Project leadership experience
• Ability to apply knowledge of statistical design, analysis and programming techniques used in clinical trials

What Plus-Project can offer you

Founded in April 2014, Plus-Project Ltd is a Biometrics CRO with offices in the UK, Europe and Asia. Plus-Project adopted Employee Ownership in 2019.  While this provided a continuation of the existing principles of employee-engagement and collaboration, the employees are rewarded equitably for the success of the business.  Fairly sharing profits with all employees, helps develop a highly engaged and enthusiastic workforce that consistently delivers excellent service levels. Employees join a happy team with a strong emphasis on continuous improvement and personal growth. Along with a competitive package, Plus-Project provide a flexible working model (including remote, office, or hybrid) and the option to purchase additional benefits.

We are committed to our team, clients, and community. We’re in this together.

How to Apply

Please click here to apply!

Plus-Project is committed to creating a diverse and inclusive workplace. We welcome applications from all qualified candidates, regardless of race, ethnicity, religion, colour, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. We are an equal opportunity employer and value the unique perspectives and experiences that each individual brings to our team.