Trial Statistician
6 month rolling contract
Switzerland
BACKGROUND
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.
RESPONSIBILITIES
* Track clinical trial / allocated project activities and milestones.
* Interact with the internal 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.
ESSENTIAL SKILLS
* At least Masters degree in Statistics (or equivalent degree).
* Fluent English, (oral and written); good communication skills.
* At least 4-6 years 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.
DESIRABLE SKILLS
* Experience in statistical modelling
* Knowledge of Bayesian design, techniques an advantage
* Knowledge of S+
* Experience with intercultural teams
For immediate consideration please forward your CV to [log in to unmask] or call...
James Carrera
Manager - Pharmaceutical Division
SEC Pharma
0044 (0) 207 225 6665
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SEC Recruitment Ltd Company registered in England and Wales No. 5808613 - Registered Office: RDL House, 1 Chertsey Road, Woking, Surrey GU21 5AD.
SEC Recruitment Ltd Company registered in England and Wales No. 5808613 - Registered Office: RDL House, 1 Chertsey Road, Woking, Surrey GU21 5AD.
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