CONTRACTOR: Senior Statistician
Switzerland
6 Months Rolling Contract
700 EURO - 830 EURO Per Day
800 - 1000 CHF Per Day
The successful candidate will be responsible for the following duties:
*Responsible for all statistical tasks on the assigned clinical trials: clinical trial design/planning, analysis plan, reporting activities including exploratory analyses, and additional analysis to support publications.
*Provide statistical consultation to clinical team and support decision making process by providing adequate information.
*Track clinical trial/allocated project activities and milestones.
*Ensure timeliness and adequate quality of all Biostatistics and Statistical Reporting deliverables for the assigned trials.
*Follow processes and adhere to client and project specific standards as well as Health Authority requirements (SOPs, Master Analysis Plan, GCP, and regulatory guidelines).
*Participate in or lead non-clinical project activities as needed.
*Application and extension of existing Bayesian methods for dose finding and proof of concept
*Establish and maintain sound working relationships and effective communication within the Clinical Trial Team and B&SR team.
Your Minimum Requirements:
Candidates applying should have the following:
*Masters Degree in Statistics (or equivalent degree) with at least 2 years of experience or PhD in Statistics (no previous experience is required).
*Knowledge and expertise in Statistics, in particular the use of applied Bayesian statistics in decision making.
*Knowledge of statistical software packages (e.g. WinBUGS, R, SAS)
*Fluent English (oral or written).
*Communicate efficiently with non-statisticians colleagues.
*Able to work with a multidisciplinary team to achieve team's objective.
DEADLINE: 16.07.2012
For a confidential consultation call Russell Gillam on 0044 (0) 207 255 6665 or email your CV to russell.gillam@secpharma.com
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