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TMG
is seeking candidates for the position of Clinical Research
Quality Manager.
-
The successful candidate's primary responsibilities will
include:
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Review,
update, distribution & tracking of TMG site Standard
Operating Procedures
-
Development
of training methods for TMG sites on SOPs/GCP
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Train
new TMG investigators and study coordinators on GCP
conduct & adherence to SOPs
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Conduct
&/or administer QA visits at TMG sites
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Manage
QA visit report results for meaningful analysis, set
standards for follow-up action
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Mentor
site study coordinators on GCP conduct issues
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Manage
new TMG initiatives on quality assurance
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Author
monthly newsletters on GCP/SOP topics of the day
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Attend
industry conferences on QA implementation for
investigators/sites
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Additional
responsibilities in keeping with the candidate's role as a
key contributor to the general management of the
organization.
Strong
candidates for the position must be detail-oriented, with
excellent communication skills and an
enthusiasm
for nurturing the development of new research professionals.
They must also have the ability to impart to experienced,
well-trained research professionals their own passion for both
learning and for clinical research.
The successful candidate must demonstrate both strong
organizational and interpersonal skills and must be
self-motivated with the proven ability to work independently
while managing multiple responsibilities.
Interested
applicants should have a minimum of 2 years of industry
experience as a CRA. Proficiency
in MS Office is required. Prior experience as a Clinical Study
Coordinator is an asset. Fluency
in French is also an asset.
Please
send your application to:
Trial
Management Group Inc.
60
St. Clair Ave. E., Suite 702
Toronto
,
ON
M4T 1N5
Attn.
John
Akitt
john@tmginvestigators.com
Phone:
416.929.7717
Fax:
416.929.4462
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