a. Number of perssonel: one legal expertise b. Place of service: provide on-site service in ICTR Beijing office c. Service term: 1 year. d. Service hours: 8 hours/day 5 working days/week e. Service level: service level: the personnel of vendors shall be capable of supporting human drug R&D activity in accordance with mutinational pharma group SOP and supervisory authority requirement. Upon receiving the assignment (legal task), deliver service (document review/creation, legal research and analysis, negotiation, report, implement legal action like dispute resolution or litigation and so forth) in qualified and timely manner which satisfies legal department and operation department requirement.
1) Personal requirements (Establish the size of the contractual effort in terms of quantities, frequencies, levels of effort, and numbers of days, weeks, months or period of a year within which contracted services or work must be preformed)
Project experience: clinical trial related legal support for multinational companies. Qualification: a. Bachelor or graduate degree is majored in law. b. Graduate from top law school; or working experience in well-known international pharma group/top law firm focusing on service for internlatioanl pharma R&D function or pass Chinese bar exame. c. Fluent in oral and written English. Capable to review English R&D contract and report to HO colleague in English.
Reporting Requirements (Describe reports and other documentation that will be required to track and demonstrate how the supplier is fulfilling the requirements of the SOW.