Talent Recruitment

Clinical Medicine Director base: Beijing Chaoyang, salary: negotiable

Job Responsibilities:

1. Responsible for the overall strategy, risk control, budget, etc. of the clinical development of innovative antibody drugs, providing comprehensive medical support for clinical trials. Participate in and supervise the design, implementation, and management of clinical projects to ensure compliance with regulatory guidelines and ethical standards;

2. Lead the completion of clinical research design and the review and execution of clinical protocols, responsible for communication and discussion with researchers, analysis of clinical data, revision and review of clinical research reports, ensuring the accuracy, high quality, and timeliness of clinical data;

3. Fully responsible for collecting industry information on related competitive product clinical development, report analysis and interpretation, deeply exploring the clinical new indications development of the company's projects. Assist external investigators and academic institutions in collaboration to obtain resources and discover potential cooperation opportunities. Participate in managing relationships with clinical research organizations (CROs), cooperative research organizations, and other relevant suppliers;

4. Independently responsible for personnel management and business assurance of the company's clinical medicine department, statistics and data department, pharmacovigilance, and other departments;

5. As the medical leader, ensure good relationships with relevant business departments, including but not limited to the drug regulatory authority, clinical research institutions, etc., provide professional medical support and ensure effective internal coordination. Responsible for leading and supervising the medical affairs team to ensure effective communication, formulation, and execution of medical plans related to the clinical development phase of R&D drugs and their clinical use after future market approval;

6. Assist other departments of the company in establishing friendly cooperative relationships with academic experts, medical experts, and industry enterprises in related fields at home and abroad, promoting the planning and implementation of project cooperation and market promotion. Represent the company at relevant medical conferences, seminars, and advisory committees, showcasing scientific data from clinical trials and promoting public awareness of the company's innovative drugs.

Job Requirements:

1. Doctorate in Clinical Medicine, Immunology, Oncology, or related life sciences, with a preference for those with a Clinical Medicine Doctor (MD) and clinical physician experience;

2. Experience working in multinational pharmaceutical companies or related biopharmaceutical enterprises, with at least 10 years of experience in innovative drug clinical development in biopharmaceuticals, biotechnology, or related industries, practical experience in clinical development of drugs for immunological diseases, and knowledge of medical affairs and clinical regulatory matters, with the ability and experience to lead corresponding teams. Proficient in clinical trial processes and relevant regulations, with experience in clinical trial monitoring management;

3. Excellent communication and presentation skills, with the ability to interact effectively and positively with internal teams and external collaborators. Ability to establish and maintain good relationships with authoritative experts in various fields, regulatory authorities, medical professionals, and patient advocacy groups.

4. Ability to focus efficiently under pressure and continuously adjust in a dynamic and fast-paced environment to ensure R&D progress.