This post is for a minimum of 6 months and based in BASEL, Switzerland.
Responsibilities will include:
- Analyses to support publications in the CVM area
- Monitoring CRO in analysis and reporting of a Phase IIIb outcome study
- Acting as Trial Statistician for assigned studies in the CVM area
Previous Experience in:
- Analysis and reporting of clinical trials
- Experience in supporting clinical publications
- Skilled in interdisciplinary work
- Strong SAS skills
- Experience in intercultural teams
You will also have a minimum of 4 years experience in pharmaceutical
development and clinical research and a minimum MS in Statistics.
Please email a cover note with an updated CV to [log in to unmask]
Kind Regards
Angie Farrell
Resourcing Manager
Chiltern International Limited
171 Bath Road
Slough
Berkshire SL1 4AA
United Kingdom
Direct Line: +44 (0) 1753 216744
Mobile: +44 (0) 778 6982644
Fax: +44 (0) 1753 511116
Website www.chiltern.com
______________________________________
IMPORTANT NOTICE
The information in this e-mail and any attached files is CONFIDENTIAL and
may be legally priviledged or prohibited from disclosure and unauthorised
use. The views of the author may not necessarily reflect those of the
Company. It is intended solely for the addressee, or the employee or
agent responsible for delivering such materials to the addressee. If you
have received this message in error please return it to the sender then
delete the e-mail and destroy any copies of it. At present the integrity
of e-mail across the Internet cannot be guaranteed and messages sent via
this medium are potentially at risk.
|