Omar López Navarrete Email and Phone Number

*Reviews and interprets documents such as clinical research protocols, site contracts, electronic CRFs and other sources of information to build the payment processing tool.* Understands in depth the protocol schedule of events (visits and procedures), contracts, budgets and payment terms to define the data that will trigger payments. * Participates in cross-functional meetings to facilitate the initial payment setup process. * Coaches new team members on established processes and… Show more *Reviews and interprets documents such as clinical research protocols, site contracts, electronic CRFs and other sources of information to build the payment processing tool.* Understands in depth the protocol schedule of events (visits and procedures), contracts, budgets and payment terms to define the data that will trigger payments. * Participates in cross-functional meetings to facilitate the initial payment setup process. * Coaches new team members on established processes and lessons learned. * Coordinates work teams for clinical trials with high volume of sites to deliver initial payment setup on time. * Understands country-specific regulations that impact the ability to make payments * Collects study information/documentation and keeps it up to date, as well as updates databases that facilitate payment processing. * Maintains an up-to-date ticketing system that tracks each request for initial setup or amendment of each research center. Show less

* Write and review regulatory information required for the authorization for the commercialization of GMOs in Mexico and Colombia. * Assembly of regulatory packages for submission to COFEPRIS, ICA and INVIMA. * Create and update databases that allow for greater clarity on authorized GMOs by regulatory authorities. * Maintain active communication with teams in the United States and Colombia to discuss deadlines for the submission of regulatory packages to the regulatory… Show more * Write and review regulatory information required for the authorization for the commercialization of GMOs in Mexico and Colombia. * Assembly of regulatory packages for submission to COFEPRIS, ICA and INVIMA. * Create and update databases that allow for greater clarity on authorized GMOs by regulatory authorities. * Maintain active communication with teams in the United States and Colombia to discuss deadlines for the submission of regulatory packages to the regulatory authorities. Show less