Legal Counsel, Clinical R&D, China

AbbVie is seeking a Legal Counsel to support its expanding Clinical Research and Development (R&D) operations in China. This role involves providing comprehensive legal guidance on Chinese and U.S. regulations pertinent to drug development, including the Drug Administration Laws, Human Genetic Resource Regulations, and Good Clinical Practice (GCP). The position is based in Shanghai and requires close collaboration with AbbVie's R&D teams to ensure compliance and facilitate efficient clinical trial processes.

The Legal Counsel will be responsible for advising on clinical research activities, encompassing patient privacy, data integrity, bioethics, and digital health. Key duties include drafting and reviewing clinical study agreements, collaborative research agreements, and service provider contracts. The role also involves developing patient informed consent forms and providing training on U.S.-China regulatory requirements to internal stakeholders.

Candidates must hold a law degree and be qualified as a PRC lawyer or possess an equivalent qualification. A minimum of seven years of legal experience in law firms or multinational corporations, with a focus on pharmaceutical or life sciences clinical development, is preferred. Proficiency in both Mandarin and English, along with a strong understanding of U.S.-China regulatory frameworks, is essential.

AbbVie offers a competitive salary and benefits package, including medical, dental, and vision insurance, paid time off, and a 401(k) plan. Employees also have access to long-term incentive programs and opportunities for professional development.

Joining AbbVie provides the opportunity to work in a dynamic and innovative environment dedicated to improving patient outcomes. The company fosters a culture of collaboration and continuous learning, offering avenues for career advancement and personal growth.