ACCURATE, ADAPTABLE, Team Player?
DEVELOPMENT RECORDS CO-ORDINATOR II
Part-Time 12 Months Temporary Contract
Cambridge Attractive Salary
At Amgen, we develop and discover important human therapeutics that bring
meaningful improvements to the lives of people all over the world. We’re
already the world’s leading independent biotechnology company, with a
turnover in excess of $3 billion.
Our success is built on innovative science, teamwork, risk-taking and the
pursuit of excellence. Key to all this is a culture where everyone is
encouraged to attain their full potential, a value system that gives
individuals the chance to make a real difference, and an environment which
has seen us recognised as one of the top 100 companies to work for by
Fortune magazine in each of the last four years.
Working within our Regulatory Affairs team, you will
· Take responsibility as records centre contact of at least one
product team
· Liaise with regulatory specialists, clinical managers and study
teams, providing records management advice
· Be responsible for co-ordinating and participating in the
classifying, scanning, indexing, filing and archiving of regulatory and
clinical study essential documents in accordance with guidelines and
procedures
· Lead and participate in departmental quality control procedures
· Have the opportunity to participate locally and internationally in
records and archiving development initiatives
· Participate in the future development and implementation of
electronic records management and storage technologies
· Provide training for staff in departmental related processes and
procedures
· Provide training and orientation for internal and global staff,
contract research organisations and external vendors on applicable
regulatory, ICH and GCP policies and procedures relevant to records
management activities
· Have an opportunity to provide support to our publishing team.
A graduate, ideally with a life science, IT or information management
qualification, you will preferably have at least two years’ relevant
experience in the pharmaceutical regulatory sector including a sound
knowledge of international regulatory requirements. Well-organised, IT-
literate and detail-conscious, you’ll demonstrate the initiative and flair
for communication to get the most out of this interesting and varied role.
In return, we’re offering a very attractive salary. To apply, please
forward your CV, together with a covering letter outlining your suitability
for the position, to: The Human Resources Department, Amgen Ltd, 240
Cambridge Science Park, Milton Road, Cambridge CB4 0WD.
E-mail: [log in to unmask]
We thank all candidates for their interest and would appreciate all
responses by Friday, 17th August 2001.
http://www.amgen.com/
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