Responsibilities:
1. Participate in developing medical strategies across the full product lifecycle, including clinical trial design, indication expansion, and post-marketing medical plans.
2. Provide clinical research support, assist in conducting clinical trials, and review study protocols, investigator brochures, and clinical study reports.
3. Address medical inquiries from study sites, ensuring that research complies with scientific and ethical standards.
4. Establish and maintain academic relationships with key opinion leaders (KOLs) in the field; organize advisory boards and academic roundtable discussions.
5. Track, collect, and analyze domestic and international clinical research developments and data relevant to the company’s products.
Qualifications:
1. Master’s degree or above in Clinical Medicine, Life Sciences, or related fields; Ph.D. preferred.
2. 3–5 years of experience in medical affairs, clinical research, or related fields.
3. Familiarity with clinical research content and processes; good knowledge of GCP.
4. Strong English skills preferred.