This position is no longer open for applications

One of my favourite clients in the food and nutrition industry is looking for an Statistician. The role is to project based for initially 6 months, starting ASAP^, for 40 hours per week. The office is located near Utrecht, with a Hybrid working policy currently in place.

Senior Clinical Statistician

Position overview

My clients is seeking a highly skilled and experienced Statistician to join their team on a temporary contract, who will be responsible for providing statistical support for clinical trials. The statistician will be responsible for designing clinical trial protocols, writing statistical analysis plans, conducting statistical analyses of clinical trial data, and generating reports to support the development of new products.

Principal responsibilities

• Support and help in development of clinical trial protocols that meet regulatory requirements, scientific objectives, and ethical principles.
• Develop statistical analysis plans, including sample size calculations, randomization procedures, and statistical methods for efficacy and safety analyses.
• Conduct statistical analyses of clinical trial data using appropriate software packages such as SAS and R.
• Collaborate with study teams and provide statistical guidance on study design, data collection, analysis and interpretation of clinical trials.
• Prepare and present statistical plans and study reports.
• Provide statistical expertise for the preparation of regulatory submissions.
• Ensure the accuracy, validity, and completeness of data analyses.
• Stay up to date with the latest statistical methods and regulatory requirements for clinical trials.

Details

• Start date: November 1^st
• Project length: 6 Months, Interim
• Location: Utrecht Area, Hybrid

About You

• A master's degree in Statistics, Biostatistics, or related fields (PhD. is preferred) with at least 5 years of experience in (clinical trial) design and analysis.
• Strong and broad knowledge of statistical methods for clinical trials, including experience with survival analysis, mixed models, and non-parametric methods.
• Experience with software packages such as SAS and R.
• Knowledge of regulatory requirements for clinical trials, including FDA, EMA , and ICH guidelines.
• Excellent communication and interpersonal skills, with the ability to work effectively in a team-oriented environment.
• Strong problem-solving skills and attention to detail.

Apply now

Are you the Clinical Data Manager I’m looking for? Please contact Tom van Marsbergen via +31 (0)20 522 1588 or t.vanmarsbergen(@)realstaffing.com