Hi
I am seeking a new candidate for a position based in Cambridge, Please
apply in confidence to Natalie Fforde
Your responsibilities will centre upon:
acting as lead statistician for individual clinical studies and liaising
closely with the lead statistician for the product in order to produce the
appropriate statistical input to study
protocols and final study reports.
contributing all statistical elements of study related documentation
including the creation of the statistical section of study protocols,
e-submissions, publications and manuscripts.
providing statistical analyses and interpretation of clinical trial data
advising non-statistical colleagues on the design requirements for studies
contributing to the project management of studies including input to study
timelines and resources
participating in the multi-disciplinary team for each project related study
SAS programming as required for a study
participating in investigator meetings
maintaining awareness of the latest statistical developments and contact
with external professional bodies
participating in the development of guidelines and SOPs for the
international Biostatistics group.
CANDIDATE PROFILE:
An undergraduate in mathematics or statistics or a related numerate
discipline. An MSc in statistics is preferred but not essential.
You must have a working knowledge of statistical methodologies and
applications within clinical trials.
Familiarity with ICH/GCP and regulatory authority statistical guidelines and
a knowledge of the clinical development process is also important.
You must have good project management and organisational skills.
Assertive, diplomatic and an excellent team player, you must be able to
communicate effectively across all disciplines.
Natalie Fforde
Director
Pharmaceutical Resourcing
Mind Consultancy Ltd
Oakfield House
35 Perrymount Road
Haywards Heath
West Sussex
RH16 3BX
Tel: +44 (0) 1444 473390
Fax: +44 (0) 1444 417874
Website: www.mind.co.uk
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