Mid-Senior Biostatistician

Looking for exciting studies to work on? Working from home availability? Want to work for prestigious and well established CRO? Looking for a 12+ months contract? If you said yes to all above, then this role is for you

The Role

The Biostatistics Contractor is a delivery focused role working under the leadership, oversight and direction of assigned Supervisor, responsible for activities relating to design, delivery and interpretation, preclinical studies, regulatory submissions and/or commercialisation. The position requires sufficient experience working as a statistician in the pharmaceutical industry, to be able to independently perform and/or lead statistical work within a study, multiple studies, indication, or be recognised as a methodology expert. This individual is able to support and/or lead work either in house or partnering externally to ensure delivery to standards, quality and time

Key Responsibilities

• Lead biostatistician role for clinical trials, ensuring protocol and regulatory compliance.

• Contribute to study synopses, protocols, and Statistical Analysis Plans (SAPs).

• Ensure the accuracy of derived datasets and contribute to clinical study reports.

• Validate randomization specifications and participate in bid defence meetings.

• Contribute statistical content to press releases and scientific papers.

• Master’s degree in statistics or biostatistics required.

• 3+ of biostatistical experience.

• Expertise in multiple statistical areas, SAS procedures, and CDISC standards desired.

• Ability to plan, supervise, and implement statistical processes for clinical trials.

• Knowledge of ICH-GCP guidelines is essential.

• Must speak Ukrainian.