Clinical Development Director

4 days ago


Singapore TRITON AI PTE LTD Full time
Overview

We are seeking an accomplished Clinical Development Director/Senior Director to join our global R&D team. Based in Singapore and reporting directly to the Group R&D Head, this individual will play a pivotal role in shaping and executing medical strategies for global market launch. The ideal candidate will bring extensive expertise in vaccine-related projects, coupled with strong regulatory knowledge and cross-border collaboration experience.

Key Responsibilities
  • Lead the design and implementation of clinical development strategies, ensuring alignment with global regulatory requirements and commercial objectives.
  • Drive clinical research programs for vaccine and therapeutic projects from early development through global launch readiness.
  • Provide scientific and medical leadership to cross-functional teams, including regulatory affairs, clinical operations, pharmacovigilance, and medical affairs.
  • Act as a key liaison with global regulatory agencies (e.g., US FDA, EMA, HSA/Health Sciences Authority Singapore) to facilitate successful clinical trial applications, approvals, and submissions.
  • Evaluate and integrate new clinical insights, emerging trends, and competitive intelligence into the company's clinical development roadmap.
  • Build and maintain strong collaborations with external KOLs, research institutions, and industry stakeholders to support global clinical programs.
  • Mentor and guide junior clinical development team members to strengthen organizational capabilities.
Qualifications & Requirements
  • MD or PhD in Medicine, Pharmacology, Immunology, or related life sciences discipline.
  • Minimum 10 years of progressive experience in clinical development within the pharmaceutical or biotechnology industry, with a strong track record in vaccine-related programs.
  • Proven experience in developing and executing global clinical development strategies, ideally from Phase I through registration.
  • Prior direct interactions and established networks with regulatory authorities such as the US FDA, European EMA, and Singapore's HSA are highly desirable.
  • Demonstrated ability to lead cross-functional and multicultural teams across global locations.
  • Strong analytical, strategic, and problem-solving skills with an ability to make sound clinical and business decisions.
  • Excellent communication and presentation skills; ability to influence senior stakeholders and external partners.
  • Fluency in both English and Chinese is required to support cross-border collaboration within the group and with international regulatory agencies.
Seniority level
  • Director
Employment type
  • Full-time
Job function
  • Research, Analyst, and Information Technology
Industries
  • Health
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