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Project management for research site coordination and oversight QCR has extensive
internal (sponsor company) and field experience in the management
and oversight of Phase I-III clinical trials both domestically
and internationally. Whether it is coordinating/interfacing
with cross-functional areas within a sponsor company related
to product development such as data management, biostatistics,
regulatory affairs and research development, or providing
field coordination between different components of a clinical
trial (e.g., central laboratory, data management, study sites),
QCR can provide expertise to ensure that your trial operations
run smoothly and efficiently. |
