Manages and executes the site identification process and performs regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements either at the global, regional, or country level.
tracks completion of regulatory and contractual documents for sites; ensures contracts are fully executed; and establishes project timelines.
Manage assigned opportunities / projects / programs for country or gegion and adhere to timelines and budget.
Ensure the site list for assigned studies includes an adequate number of appropriate investigators in accordance with the needs of the sponsor and specificataions of the protocol.
Collect and analyze country / regional Feasibility and / or Site Identification information to meet timelines of each study.
Attend kick off meetigs to understand study requirements include investigator profile, protocol, process speoifics and timelines.
Raise questions and make suggestions based on SID SOPs and Work Instructions.
Distribute, track and review Site Questionaires for Feasibility and / or Site Information Forms or Site Qualification Questionaires for SID .
Enusre completenes, site capability and suitability fo rthe study.
3 years clinical research experience. Equivalent combination of education, training and experience.
Advanced leve lof English.
intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience