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Investigator
Services
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Quality
studies are a result of quality planning
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At Pivotal Research Solutions,
your clinical trial study will be placed in the
hands of dedicated team of clinical research professionals
that will manage every aspect of your study
Pivotal's Solutions
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- A fully integrated
team dedicated to the success of your
clinical trial
- Open lines of communication
with a single reference point for investigators
and sponsors
- Quality control measures
at every juncture of your trial
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Study Initiation
Pivotal Research will work
with the sponsor to develop investigator sites,
to collect essential documents and negotiate clinical
study agreements.
Documentation Maintenance
Pivotal Research’s quality
control staff is responsible for the maintenance
of all essential documentation for each investigator
in the study. This documentation may include clinical
trial agreements, financial disclosures, IRB approvals
and personnel credentials, and is maintained at
Pivotal Research’s corporate offices for the
duration of the study. Copies are forwarded to sponsors
or managed offsite.
Conversely, the quality control staff is also responsible
for distribution of important documentation to each
site, including protocol amendments, updated literature
safety reports, and other materials that may be
related to the study or the site.
Clinical Study Agreements
Pivotal Research works with
the sponsor to finalize individual clinical study
agreements for each site in a timely fashion.
Grants Management
Once clinical trial agreements
are in place, Pivotal manages the budgetary issues
associated with each site and provides timely payment
to sites for completed work statements, as specified
in the agreement.
Investigator Meeting Coordination
Our marketing management
staff has extensive program development and meeting
venue experience and can coordinate the investigator
meeting arrangements, including pre-meeting and
on-site management services for investigators and
sponsors.
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