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| Site Contracts and Payments |
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| The DCRI offers comprehensive site contracts
and payments services, from contract negotiation to detailed
payment reporting and database maintenance. Our experience with
trials of all sizes, from small domestic studies to global megatrials,
gives the DCRI the ability to customize site payment and contract
processes to a sponsor’s needs.
Our Contracts Management and Finance experts all work closely
with our sponsors, and with one another, to create a coordinated
process for site contract execution and payments. This collaboration
means the DCRI can negotiate site contracts on the sponsor’s
behalf, using time-tested templates and methods, all refined
through extensive consultation between our sponsors and our
experienced personnel.
DCRI’s Contracts Management group employs a team of
six contract specialists, managed by a site team manager with
over 15 years in the field of contracts management. Each contract
specialist has over two years of experience in the negotiation
and administration of clinical study agreements. Three contract
specialists have graduate degrees in either the law or healthcare
administration. To ensure that the negotiation process goes
smoothly and that the outcomes are consistent with our clients’
requirements, a senior attorney is also assigned to each study
and acts as the primary interface with the client. All senior
attorneys have over 10 years of experience in contract management,
some much more. All of our attorneys are licensed and members
of various state bars.
Contacts:
Site Contracts: Betsy Reid, CBO (Interim)
Site Payments: Michael Sledge, CFO
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| Our dedication to our clients’
needs is evident in the calculation, processing, and reporting
of payments. An integrated database that allows our groups
to work seamlessly together generates payment reports using
pre-determined milestones or specific event triggers derived
from our data management system. These reports can be detailed,
patient-by-patient documents or cumulative reports made monthly,
quarterly, or any time period our sponsor requires. The wealth
of information provided not only gives our sponsors fiscal
peace of mind, but also ensures a smoothly executed trial
that encourages swift enrollment and responsiveness from participating
sites.
Proven DCRI processes and attention to detail, even on the
global scale, give us the ability to negotiate with individual
sites and execute individual agreements without compromising
the needs of our clients or inhibiting sites’ abilities
to initiate the study and begin to enroll patients.
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