Senior Statistician - Oncology Specialist
European Medical Support
£ Excellent Salary + Benefits
Job Summary:
The Senior statistician will support European Medical Colleagues in collaboration and under functional supervision of the US parent company in order to facilitate common working practices and to share knowledge / experience.
Accountabilities/Responsibilities:
* Post-hoc statistical analyses to support International regulatory filings, publication planning and health economic analyses.
* Provide face-to-face statistical input for projects to which he is assigned
* Provide statistical input into the design of protocols including preparation of the biostatistical analysis section.
* Prepare statistical analysis plans including table shells.
* Analyze and report results of clinical trials. Provide tables, listings and graphs for final study reports.
* Manage outside CROs and consultants.
Essential Skills & Capabilities:
MS/PH.D. in Statistics with at least x years experience as a statistician supporting clinical trials in the pharmaceutical industry or similar academic institution
§ Master's Degree/Ph.D. in statistics with focus on statistical methods appropriate for clinical trials.
§ Demonstrated skills and experience in a statistical department including direct interaction with clinical personnel in the planning, analysis and reporting of clinical trials either in a pharmaceutical industry or similar academic setting
§ Experience with working on an NDA or sNDA is desirable, but not required.
§ Detailed knowledge of statistical regulatory requirements
§ Excellent SAS skills including report generation.
§ Knowledge of MS Office products (Word, Excel)
§ Experience in oncology trials would be an asset.
§ Excellent interpersonal, communication, writing and organizational skills.
§ Demonstrated ability to work in a team environment with medical personnel, clinical monitors, data managers, programmers and medical writers.
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 0044 (0) 207 255 6665 or email your CV to [log in to unmask]
James Carrera
European Contracts Manager
Pharmaceutical, Healthcare & CRO division
1st Pharma People
"A Division of 1st IT People"
Tel: +44 (0) 207 255 6665
Fax: +44 (0) 207 255 6656
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www.1st-pharmapeople.com
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