Dear All
An excellent opportunity has arisen this pharmaceutical client based in
Germany;
Manager Statistical Programming
Your Responsibilities:
- To manage and supervise a small group of statistical programmers plus
variable number of contract statistical programmers
- To ensure the development and maintenance of programming standards and
standard programs for the reporting of phase II - IV clinical trials
- To ensure the correct and efficient programming of analyses for
pan-European and US phase II -IV clinical trials as required, e.g. end of
study reports, submission reports
- To ensure that the statistical programming is performed accordingly to
good clinical practice and regulatory standards
Your Profile:
- Degree or technical qualification in computing, statistics, mathematics,
medical documentation or related discipline
- At least 5 years of programming experience with SAS
- Minimum of 3 years working experience in data management or biometrics
group within the pharmaceutical industry or a CRO
- Active contributions to the programming of end of study reports and/or
major contributions to the development of standard programs in SAS
- Excellent English language skills (written and spoken)
- Excellent managerial, communication and presentation skills
Please send cv or call me for further information.
Regards
Shaun Richards
Senior Permanent Consultant
Pharmaceutical, Healthcare & CRO division.
1st IT People
Tel: +44 (0) 207 940 3900
Fax: +44 (0) 207 407 8288
mailto:[log in to unmask]
www.1st-itpeople.com
Offices in UK, Switzerland, The Netherlands & Hong Kong
|