Our client is a large global pharma company with a highly respected R&D
facility in the UK. This role has been created to meet the increasing
demands of a strong pipeline of exciting products.
MAIN PURPOSE OF ROLE:
* To define, design and review the statistical section of protocols
and clinical reports.
* To monitor, manage and control CRO activities to ensure that
project/study milestones are met within agreed time, cost, resource and
quality parameters.
REQUIREMENTS:
Graduate with relevant additional higher tertiary qualification
At least 3 years statistics experience in a CRO or mainstream pharma
Will have evaluated large clinical studies involving patient numbers in
excess of 100
Will have worked on clinical trials in different phases particularly Phase
III
Regular European and international exposure - comfortable in a multicultural
environment
Will have had exposure to the rigours of the regulatory authorities
Will have led the development of statistical analysis plans and reviewing
final reports
Please contact:
By return of email or call James Thompson on 07973 229 753 for a
confidential discussion.
This e-mail and any files transmitted with it are confidential (and may contain privileged
information) to the ordinary user of the e-mail address to which it was addresses and must
not be copied, disclosed or distributed without the prior authorisation of the sender.
Please notify the sender and destroy this e-mail immediately if you are not the intended recipient.
Please also note that while our own software systems have been used to try to ensure
that this e-mail has been swept for viruses, we do not accept responsibility for any
damage or loss caused in respect of any viruses transmitted by the e-mail.
Please ensure your own checks are carried out before any attachments are opened.
|