Legal Counsel, Clinical R&D, China
Core
Provide dedicated legal support for AbbVie's R&D activities in China, advising on Chinese laws, regulations, and U.S. frameworks like the BIOSECURE Act and Bulk Data Transfer Rule.
Role type
Legal Counsel (Clinical R&D)
Builds
Legal guidance for clinical research, drug development pipelines, and regulatory filings in China.
Domain
Life Sciences / Pharma / Clinical R&D
Required skills
Chinese law expertise, U.S.-China regulatory frameworks, clinical trial design, contract drafting, health authority engagement, patient informed consent, regulatory tracking, legal analysis
Preferred skills
Pharma/life sciences background, FDA approval familiarity, cross-functional collaboration
Technologies
None stated
Responsibilities
Advise on Chinese laws and U.S. regulations (BIOSECURE Act, Bulk Data Transfer Rule); Develop legal guidance for clinical research; Support end-to-end R&D from trial design to pre-commercialization; Draft and review clinical study and collaborative agreements; Develop patient informed consent forms; Track regulatory developments; Provide training on U.S.-China requirements
Seniority
Mid-Senior, hands-on IC
