CONTRACT: Biostatistician - Mainland Europe - Accommodation Provided
12 month rolling contract
Job Summary:
Working for one of the worlds largest Biotech companies in a simply
fantastic city. You will work as a Biostatistician on a 12 month rolling
contract for which my client will provide you with an apartment for the
duration of your stay.
Accountabilities/Responsibilities:
* Provide statistical input for protocol/CRF development (e.g.,
design; appropriate collection of observations in order to satisfy
objectives; sample size estimation for the most efficient and practical
design; patient randomization; accurate, logical, clear, concise and
thorough evaluation of results section; effective CRF specifications to
collect data specified in the protocol) and query checks.
* Write analysis plans for clinical trials including the most
appropriate statistical methodology and data presentations.
* Write accurate, logical, clear, concise, thorough and objective
statistical methods sections for integrated final reports.
* Review integrated draft reports ensuring the accuracy of the
statistics.
* Perform statistical analysis for manuscripts
* Keep abreast of statistical developments
* Program and validate tables and derived listings as required.
* Understand and follow all statistical and statistical programming
SOPs as well as any other relevant SOP.
* Communicate statistical concepts and results to non-statistical
internal colleagues in a clear, concise, focused and articulate manner.
* Provide leadership to non-statistical colleagues with statistical
issues
Essential Skills & Capabilities:
Minimum 2-4 years experience of statistics in a clinical trial environment.
Advanced degree (MSc or PhD) in statistics, biostatistics, mathematics, or
related field, BSc qualifications will be considered with good relevant
industry and statistical experience.
SAS programming skills are also required.
* Strong knowledge of statistical principles, and strong statistical
skills.
* SAS programming skills and understanding of database structures.
* Good organizational skills across multiple projects, managing own
and team workloads. The ability to adapt and adjust to changing priorities.
* Excellent written and verbal communication skills.
* Ability to work in a multi-disciplinary team setting.
* Demonstrated initiative, motivation and problem solving skills.
An excellent opportunity awaits for this renewable contract. Interview times
booked and full job specification to review...
If you would to discuss this role in greater detail or your application /
suitability to this or further roles, please call me or email me in
confidence. If you are not available or suited to this position, please feel
free to pass my details on.
We also have a broad variety of other Biometric specific vacancies available
in the UK and throughout Europe. Inclusive of SAS programming, Statistical,
Clinical programming, Data Management functions, Regulatory Affairs,
Clinical Research, QA, Compliance & Validation.
For a confidential consultation call James Carrera on; 0207 255 6665
James Carrera
European Contracts Manager
Pharmaceutical, Healthcare & CRO division
1st Pharma People
"A Division of 1st IT People"
Tel: +44 (0) 207 255 6665
Mobile: +44 7717 578 246
Fax: +44 (0) 207 255 6656
mailto:[log in to unmask]
www.1st-pharmapeople.com
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