Dear Allstat
SRG Clinical have an urgent requirement for an experienced Trial
Statistician to fulfill a 6+ month assignment with a blue-chip pharma in
Switzerland:
Responsibilities Include:
* Responsible for all statistical tasks of the assigned clinical
studies e.g. clinical trial design/planning, analysis plan, reporting
activities, support to publications, and any statistical consultation
during the running phase.
* Track clinical trial / allocated project activities and
milestones.
* Interact with the Methodology group as appropriate.
* Ensure timelines and adequate quality of all Biostatistics and
Statistical Reporting deliverables for the assigned trials and project
task.
* Follow processes and adhere to project specific standards as
well as Health Authority requirements (SOPs, Master Analysis Plan, full
development project specifications, and regulatory guidelines).
* Establish and maintain sound working relationships and effective
communication within the clinical trial team and the Clinical
Information Sciences (CIS) team.
Experience and Qualifications:
* At least Masters degree in Statistics (or equivalent degree).
* Fluent English, (oral and written); good communication skills.
* Significant relevant experience required, including experience
in Pharma.
* Knowledge of statistical software packages; strong knowledge of
SAS
* High Degree of autonomy in performing assigned duties.
* Knowledge of drug development process.
You must be eligible to work in the EEA and posses excellent written and
oral English skills. Please call Helena on +44 (0)7825362548 or email
your CV to [log in to unmask]
Best wishes
Helena
Helena Newman-Mitchell
Biometrics Lead
Direct: +44 (0) 207 562 1792
Fax: +44 (0) 207 562 1799
Mobile: +44 (0) 782 536 2548
Email: [log in to unmask]
Website: www.srgclinical.com <http://www.srgclinical.com/>
5th Floor, 5 Devonshire Sq, London, EC2M 4YD
Please note I work Monday - Thursday
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