
Global Clinical Development Leader
6 days ago
As a seasoned medical professional, you will lead the development of clinical strategies that align with global regulatory requirements and commercial objectives. Your expertise in vaccine-related projects, coupled with strong knowledge of regulatory affairs and cross-border collaboration experience, will drive clinical research programs from early development through global launch readiness.
">Key Responsibilities:- You will oversee the design and implementation of clinical trials, ensuring compliance with international regulations and company standards.
- Your role will involve providing scientific and medical leadership to cross-functional teams, including regulatory affairs, clinical operations, pharmacovigilance, and medical affairs.
- You will act as a key liaison with global regulatory agencies, facilitating successful clinical trial applications, approvals, and submissions.
- Your task will be to evaluate and integrate new clinical insights, emerging trends, and competitive intelligence into the company's clinical development roadmap.
- You will build and maintain strong collaborations with external key opinion leaders, research institutions, and industry stakeholders to support global clinical programs.
- Additionally, you will mentor and guide junior clinical development team members to strengthen organizational capabilities.
We are seeking an accomplished Clinical Development Director/Senior Director to join our global R&D team. The ideal candidate will bring extensive experience in leading cross-functional and multicultural teams across global locations. Strong analytical, strategic, and problem-solving skills, along with excellent communication and presentation skills, are essential for this role.
The successful candidate will have a minimum of 10 years of progressive experience in clinical development within the pharmaceutical or biotechnology industry, with a strong track record in vaccine-related programs. A MD or PhD in Medicine, Pharmacology, Immunology, or related life sciences discipline is required. Fluency in both English and Chinese is necessary to support cross-border collaboration within the group and with international regulatory agencies.
Seniority level:- Director
- Full-time
- Research, Analyst, and Information Technology
- Health
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