1. Providing Flexible Resourcing Solutions
CTC Resourcing Solutions, founded in Basel, Switzerland in 1997, is a specialist staffing organisation based in
Basel, London and Munich, providing flexible resourcing solutions to the pharmaceutical industry across Europe,
with contract and permanent placements in clinical development, data management, statistics, regulatory affairs
and medical marketing.
For one of our clients, we are currently looking for a
Senior Statistician
Reference Number: 10-13-794-SS-W
Type of placement: Permanent
Location: Basel, Switzerland
Purpose:
To be responsible for all statistical tasks of individual clinical trials. He/she may take on project level
tasks of a Program Statistician, initially under the supervision of a more experienced Statistician/Group
Head but with increasing autonomy and accountability.
Main Responsibilities:
 Be responsible for all statistical tasks on the assigned clinical trials, and perform these tasks
with a high level of independence e.g.: clinical trial design/planning, analysis plan, reporting
activities including exploratory analyses and additional analyses to support publications, plus
statistical consultation during the running phase.
 May be assigned to lead a small project or parts (e.g. indication) of a project, initially under the
guidance of a more experienced statistician, but with increasing autonomy and accountability.
 Track clinical trial/allocated project activities and milestones.
 Ensure timeliness and adequate quality of all Biostatistics and Statistical Reporting deliverables
for the assigned trials and project tasks.
 Follow processes and adhere to project specific standards as well as Health Authority (HA)
requirements, SOPs, Master Analysis Plan, GCP, and regulatory guidelines.
 Participate in or lead non-clinical project activities as needed.
 Establish and maintain sound working relationships and effective communication within the
Clinical Trial Team and the Biostatistics & Statistics team.
Qualifications and Experience:
 At least Masters Degree in Statistics (or equivalent degree) with 5 years of experience or PhD
with 2-3 years of experience.
 Experience in all tasks of a Trial Statistician. Proven knowledge in Statistics and its applications
to clinical trials.
 Proven knowledge of drug development and HA guidelines.
 Background medical knowledge, preferably in relation to the specific therapeutic area.
 Proven knowledge of statistical software packages.
 Good communication and presentation skills.
 Good team player.
 Fluent in both written and spoken English
 Relevant working/residency permit or Swiss/EU-Citizenship required
Our offer:
 Competitive salary and package

2.  Wide range of career opportunities in a large pharmaceutical organisation
 International experience
Should you be interested in the above position and wish to apply, please send your application with your CV,
quoting the above reference number, to our recruitment team at recruitment@ctcon.ch
CTC Clinical Trial Consulting, Greifengasse 1, CH 4058 Basel, Switzerland
Tel.: +41 61 695 88 66 Fax: +41 61 695 88 67 www.ctcon.ch info@ctcon.ch