


Pharmaceutical Product Development
Position
Summary:
Performs
data management activities in support of clinical studies including
pre-entry review, data validation, query management and quality
control of the data and project deliverables.
Major
Responsibilities:
Performs
pre-entry review of CRFs
Performs
data validation using both electronic and manual checks or
listings
Performs
query management including creation, review and update of
database
Performs
various quality control activities of data and project
deliverables
If
appropriate, participates in user acceptance testing of clinical
databases
Participates
in internal team meetings as necessary
Performs
Senior Clinical Data Support Associate activities as needed
Performs other duties as assigned
Skills
Required:
Good
working knowledge of clinical trials and data management's role
in the clinical trials process
Ability
to work well in a team environment
Excellent
attention to detail
Good
analytical, organisational and problem-solving abilities, and
ability to prioritise multiple tasks
Dedication
to quality in all aspects of work
Flexibility
Good
judgment skills
Ability
to use initiative effectively
Works
well with moderate supervision
Self-motivation
and ability to function independently
Ability
to function effectively under pressure
Knowledge
of Microsoft Word, Excel and Powerpoint
Effective
communications skills, both written and verbal
Good
command of the English language
Oracle Clinical experience preferable
Education
or Equivalent Experience:
Bachelor's
degree in applied or life science
Typically
minimum of 1 year experience in clinical trials (with at least 6
months in data management)
or equivalent education and work experience
To
apply for this position please send your CV to recruituk@constellagroup.com
if you have any questions please do not hesitate to call us on 01235
437 624