A global clinical research organization is seeking a Country Approval Specialist based in Buenos Aires, Argentina.... This role is essential for coordinating regulatory submissions and ensuring site activation. The successful candidate will need...
A integral clinical research organization is seeking a Country Approval Specialist based in Buenos Aires, Argentina.... This role is essential for coordinating regulatory submissions and ensuring site activation. The successful candidate will need...
, you are responsible for pulling regulatory country submissions together in order to activate investigative sites... around the world to decrease startup timelines and exceed expectations. Summarized Purpose As a Country Approval Specialist...
, you are responsible for pulling regulatory country submissions together in order to activate investigative sites... around the world to decrease startup timelines and exceed expectations. Summarized Purpose As a Country Approval Specialist...
, you are responsible for pulling regulatory country submissions together in order to activate investigative sites... around the world to decrease startup timelines and exceed expectations. Summarized Purpose As a Country Approval Specialist...
, you are responsible for pulling regulatory country submissions together in order to activate investigative sites... around the world to decrease startup timelines and exceed expectations. Summarized Purpose As a Country Approval Specialist...
regulatory authorities as required by countries and in accordance with ICH/GCP and applicable country regulations/guidelines..., including submissions to regulatory authorities and ethics committees. Ability to read and understand clinical protocols...
Submissions Specialist - Follows the project direction provided by the designated country start-up advisor (CSA) and SAM. May... required by central and local EC and RA, and other local regulatory authorities as needed within the country; includes safety...