Statistician – Pharmaceutical / Clinical Trials
Full job description
CG CONSULTANTS
Statistician – Pharmaceutical / Clinical Trials
Are you a Statistician? Do you have experience working with in CRO / Pharmaceutical environment? Do you have experience with clinical trials stage I /II and an excellent understanding of PK and statistical reposting? If so a leader in the manufacture and development of niche pharmaceuticals are looking to speak to you. Initially a 12 month contract you will be responsible for supporting the statistical data across all early stage clinical trials.
THE SALARY/RATE/PACKAGE/BENEFITS
Statistician – Pharmaceutical / Clinical Trials
• Highly Competitive daily rate
• Start ASAP
• Initial 12 month contract
THE CANDIDATE
Statistician – Pharmaceutical / Clinical Trials
• Degree qualified in Statistics or a similar data driven subject
• Extensive experience working in a similar position within a pharmaceutical or clinical research organisation
• Good understanding of regulatory requirements and guidelines
• Good knowledge of SAS and some experience with programming would be ideal
THE ROLE
Statistician – Pharmaceutical / Clinical Trials
You will be responsible for statistics relating to clinical trials data from the next wave of products in development. Working closely with study teams you will take responsibility for Statistical input from inception through to reporting of phase I, II and III studies providing your expert analysis on the data, interpreting results and ensuring data validity. You will also ensure all data is compliant with the relevant standards and will take responsibility for responding to regulatory questions on submissions.
REFERRAL INFORMATION
Please submit your CV via email to apply in the first instance. We offer referral fees to those recommending unique applicants we go on to place. Do you know anyone suitable?
Location: Cambridge, Haverhill, Bedford, Harlow, Cambridgeshire
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