Salary: 80-110k
Experience requirements:Over 10 years
Educational requirements:PhD
Job Description:
Job Responsibilities:
1. Responsible for the overall strategy, risk control, budget, etc. of 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 and ethical standards
2. Lead the completion of clinical research design and the review and implementation of clinical protocols, responsible for communicating and discussing with researchers, analyzing clinical data, revising and reviewing clinical research reports, ensuring the accuracy, high quality, and timeliness of clinical data
3. Fully responsible for collecting industry information, analyzing and interpreting reports related to the clinical development of competitors, and deeply exploring the development of new clinical indications for the company's projects. Assist external investigators and academic institutions in collaborating to obtain resources and identify potential opportunities for collaboration. Participate in managing relationships with clinical research organizations (CROs), collaborative research organizations, and other related suppliers
4. Independently responsible for personnel management and business assurance of the company's Clinical Medicine Department, Statistics and Data Department, Pharmacovigilance Department, and other departments
5. As the medical manager, ensure the establishment of good relationships with relevant business departments, including but not limited to drug regulatory agencies, clinical research institutions, etc., provide professional medical support, and coordinate effectively internally. Responsible for leading and supervising the medical affairs team to ensure effective communication, formulation, and execution of medical plans related to the clinical use of research and development drugs during the clinical development phase and after future approval for market launch
6. Assist other departments of the company in establishing friendly cooperative relationships with academic experts, medical experts, and industry enterprises in relevant fields at home and abroad, and promote the planning, implementation, and market promotion of project cooperation. Representing the company in 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. Doctoral degrees in clinical medicine, immunology, oncology, or related life sciences, as well as a Doctor of Clinical Medicine (MD) with clinical experience, are given priority consideration
2. Having work experience in multinational pharmaceutical companies or related biopharmaceutical enterprises, with at least 10 years of clinical development experience in innovative drugs in biopharmaceuticals, biotechnology, or related industries, practical experience in clinical development of drugs for immunology related diseases, and professional knowledge in medical affairs and clinical supervision, as well as the ability and experience to lead corresponding teams. Proficient in clinical trial procedures and relevant regulations, with experience in clinical trial supervision and management
3. Has excellent communication and presentation skills, and the ability to effectively and positively interact with internal teams and external collaborators. Ability to establish and maintain good relationships with authoritative experts, pharmaceutical regulatory authorities, medical professionals, and patient rights groups in various fields
4. Ability to focus efficiently under pressure and continuously adjust in a dynamic and fast-paced environment to ensure research and development progress