Cluster Head, Medical

22 hours ago

Singapore DKSH Full time

Overview

The Cluster Head, Medical & Regulatory Affairs, South East Asia (SEA) based in Singapore provides strategic leadership and operational oversight across Medical and Regulatory Affairs in the region. Leading a team of country medical and regulatory heads, the role ensures scientific integrity, medical governance, regulatory compliance, and cross-functional collaboration to support the portfolio across its lifecycle. This position serves as the key interface between global/regional leadership and local country operations, aligning strategies with business priorities while adapting to local market and regulatory environments.

Responsibilities

  • Strategic Leadership: Define and execute cluster-wide medical and regulatory strategies aligned with overall business objectives.
  • Medical & Regulatory Affairs: Drive medical excellence across the cluster, ensuring scientific engagement and alignment with therapeutic area strategies; oversee regulatory submissions, registrations, and lifecycle management across SEA markets.
  • Cross-functional Collaboration: Partner with commercial, market access, and other cross-functional teams to deliver integrated business planning and execution; provide medical and regulatory insights to support business development and partnership opportunities.
  • Governance & Compliance: Establish and maintain robust quality systems and regulatory governance frameworks in line with global risk and compliance standards; monitor regulatory intelligence and adapt strategies to evolving policies and market dynamics.
  • Talent Development & Leadership: Coach and mentor country medical and regulatory leaders, building high-performing teams; ensure succession planning, capability development, and a culture of accountability and excellence across the cluster.
  • External Engagement: Represent the company in industry associations, regulatory forums, and scientific discussions; build strong relationships with key opinion leaders, regulators, and external partners to shape the external environment and support strategic partnerships.

Qualifications

  • Advanced degree in life sciences (MD, PhD, PharmD, or equivalent) strongly preferred.
  • 10+ years of experience in medical affairs and regulatory affairs within the pharmaceutical or biotech industry.
  • Proven regional or cross-country leadership experience in a matrixed organization.
  • Strong leadership skills with demonstrated success in talent development and team engagement.
  • Deep understanding of customer needs, regulatory dynamics, and evolving market environments in SEA.

Job Details

  • Seniority level: Executive
  • Employment type: Full-time
  • Industries: Pharmaceutical Manufacturing; Retail Pharmacies; Medical Equipment Manufacturing
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