This role is based with a client in the USA. The ideal candidate MUST have
good FDA knowledge
Th ideal candidate requires a Ph.D. in Biostatistics, or in science with
statistics minor, or Masters equivalent plus five to seven years design
and analysis of clinical trials experience in a Contract Research
Organization or Pharmaceutical/Biotechnology company, including three
years managing a biostatistics group. Neurology/central nervous system
experience is preferred. Requires in-depth knowledge of FDA regulations
and experience in interacting with the FDA. Working knowledge of major
statistical software programs, e.g. SAS, StatXact, Nonlin, EaSt, etc., is
necessary. Data management experience is a plus. Ability to handle
multiple tasks to meet deadlines in a dynamic environment is essential.
Requires effective organizational, presentation, documentation and
interpersonal skills with demonstrated ability to lead and motivate a
group. Basic computer skills in Word, Excel and Lotus Notes are necessary
Please contact Natalie Fforde if you are interested in a move....
Natalie Fforde
Curtis House
34 Third Ave
Hove
BN3 2PD
Tel: 01273 722366
Fax: 01273 325350
Mobile: 07769 700 222
Email: [log in to unmask]
www.fforde-management.com
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