Senior Statistical Scientist

Senior Statistical Scientist

UK or EU (Remote or hybrid)

£65,000 - £75,000 pa + generous benefits package and bonus

Application deadline: 14th November 2022

Please apply directly by CV submission or contact me on the details below for a confidential discussion.

Highlight of key skills required: SAS and/or R, CDISC (sdtm/adam), clinical trial design (adaptive design), CRO/pharma experience, and minimum of MSc in Stats

The company/team:

This unique and specialised role forms part of the consultancy team in a global-reach business. The company is leading in the industry and there is copious amounts of opportunities to develop and learn. This statistical research team supports clinical development, endpoint selections, sample size estimation, simulations, advise on unique design and analysis, and assist with data displays and interpretations of data analysis results, based on machine learning/ complex data.

The role:

• You will work as a statistical consultant, supporting clients internally and externally
• You will serve as a SME and specialise in your area of choice in statistical leadership
• You may be involved in data monitoring committees
• You will engage in publishing papers, editorial works and giving presentations at conferences
• This specific groups expertise in design types include: biosimilars, adaptive designs, seamless designs, dose-response designs, master protocols, Bayesian methods and analyses.
• You will collaborate with different teams that include medical, regulatory, pharmacokinetic, and operational experts.

The required skills:

• MSc and/or PhD degree in Biostatistics or related
• Minimum of 6 years experience within the life-sciences industry either pharma or CRO
• Experience with clinical trial design (specifically adaptive design)
• Excellent working knowledge of advanced/complex statistical techniques
• Experience correct implementing and applying statistical methods in clinical trials
• Strong experience with SAS and/or R
• Experience working with CDSIC (sdtm and adam)
• Work experience with regulatory bodies such as FDA, EMEA etc