Please find details of a contract opportunity I have in Mainland Europe.
Please forward me you resume in the first instance or feel free to call for
an informal chat.
Kind Regards,
Ian
MDM/EDM e-CRF developer
Working within an international group of e-CRF development specialists and
in close cooperation with clinical teams you will be trained in a newly
developed, modern software which you will use for the design of electronic
CRF applications to facilitate speedy collection of high quality and
validated data from clinical trials at the investigational sites.
You will also prepare for the transfer, storage and further processing of
the data within a central data-repository.
To fulfil this role you will
Closely cooperate with the Data Manager and the clinical team to design the
layout and optimal functionality of the electronic CRF pages as required by
the clinical protocol
Program validation checks to ensure high quality and integrity of the
clinical data
Contribute to the development of global and TA specific standard e-CRFs
Develop a complementary clinical database structure within a central
data-repository
Prepare specifications for the transfer of the data from the EDC system
into the central database and test the transfer programs
Ensure that clinical database standards are developed for new and adhered
to for existing clinical projects
Develop validation reports with SAS or equivalent reporting tools to
complement the cleaning of the data
The ideal candidate is likely to have a degree in life sciences or medical
informatics, preferably supported by a postgraduate qualification and
should have experience in the set-up and design of clinical databases with
at least one major Clinical Data Management system (e.g. CT4 or Oracle
Clinical). Your experience will extend beyond 3 years in drug development,
with typically at least 2 years of experience in clinical programming and
clinical database design.
To achieve the level of performance that we are expecting, you will bring
with you a thorough understanding of clinical trial methodology, GCP and
medical terminology. You should feel committed to high quality work, feel
comfortable working in international teams, should have good communication
skills and be prepared to cope with occasional high time pressure.
Mind Consultancy Ltd
Oakfield House
35 Perrymount Road
Haywards Heath
West Sussex
RH16 3BX
www.mind.co.uk
Tel: +44 (0) 1444 473390
Fax: +44 (0) 1444 417874
__________________________________________________________________________
This transmission has been issued by Mind Consultancy Ltd for the
information of the addressee only and should not be reproduced and / or
distributed to any other person. Unless otherwise agreed in writing, any CV
or Candidate details attached hereto must be read in conjunction with, and
are subject to, Mind Consultancy's Standard Terms of Business. Its contents
are based on information obtained from sources believed to be reliable but
Mind makes no representation and accepts no responsibility or liability as
to its completeness or accuracy.
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