Senior Biostatistician for Pharmaceutical Development

4 days ago


Stirling, Stirling, United Kingdom Lifelancer Full time

ClinChoice is a global full-service Contract Research Organization (CRO) specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 28 years of proven high-quality delivery and results across all our services, we have a strong focus on quality, professional development, and a supportive culture.

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset, and we provide close management and training to develop and maintain highly-qualified personnel. The continuous training keeps our resources qualified in terms of competence and expertise, giving them the clear tools needed to manage both internal and client processes with the same methodology.

We are an equal opportunity employer, committed to attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this as our strength and celebrate it.

The successful candidate will be responsible for protocol development, including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies. They will also provide statistical oversight to studies and assure adequate quality and consistency with project requirements.

The salary for this position is approximately £80,000 - £100,000 per year, depending on experience. If you have a Master's or PhD in Statistics, Biostatistics, or a related field, with 7-8 years of experience or 3-5 years of experience respectively, and a strong understanding of statistical concepts and methodologies, we encourage you to apply.

As a Senior Biostatistician at ClinChoice, you will work on various projects, including clinical trials, and interact with Regulatory Agencies. You will be responsible for assuring that data for statistical analyses are complete, accurate, and consistent. You will also be responsible for statistical analysis plans and the accuracy and timeliness of statistical input into reports or decisions.

To succeed in this role, you should have excellent communication skills, both written and oral. You should be able to effectively communicate with clients and colleagues, and mentor peers with regards to statistical methodology. You should also be able to manage activities of statisticians across projects by coordinating assignments and reviewing work so that projects are delivered on time with high quality.



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