Title:  IVD Senior Regional Scientific Manager, Thailand

IVD Senior Regional Scientific Manager, Thailand will lead scientific and clinical initiatives to strengthen Mindray’s position in the IVD market. This role is responsible for identifying, managing, and supporting clinical studies in Thailand, building strong relationships with Key Opinion Leaders, and ensuring compliance with regulatory and ethical standards. Acting as a bridge between HQ Scientific Affairs team, APAC/Thailand Marketing team, and external stakeholders, the IVD Senior Regional Scientific Manager, Thailand will drive evidence-based strategies that support product adoption and market growth, including scientific publications and presentations.

Responsibilities

Clinical Studies Management

• Identify and initiate clinical study opportunities at Thailand level in collaboration with HQ Scientific team and APAC/local Marketing teams.
• Manage study agreements, timelines, and deliverables.
• Ensure compliance with ethical committees and regulatory requirements.

KOLs Development

• Identify and engage new Key Opinion Leaders in Thailand.
• Build and maintain strong relationships with scientific and clinical experts.

Scientific Support & Publications

• Support the development of scientific publications, abstracts, and presentations based on clinical evidence.

• Collaborate with internal and external stakeholders to ensure high-quality scientific content.

Stakeholder Collaboration

• Work closely with HQ, local Product Specialists, and marketing team to align scientific initiatives with business objectives.
• Negotiate and manage agreements with university hospitals and research institutions.

Compliance & Documentation

• Prepare and review study protocols, agreements, and ethical submissions.
• Ensure adherence to internal and external compliance standards.

Reporting & Communication

• Report regularly to Regional Marketing manager and HQ Scientific Affairs Manager on the status of the clinical studies in Thailand.
• Provide insights and recommendations for continuous improvement.
• Ensure timely communication of key updates and challenges.

Skills 

• Strong knowledge of IVD industry and clinical study processes.
• Excellent understanding of regulatory and ethical requirements for clinical research.
• Ability to negotiate and manage agreements with hospitals and academic institutions.
• Experience in scientific writing and publication processes (peer-reviewed journals, congress abstracts).
• Strong communication and relationship-building skills.
• Project management and organizational skills to handle multiple studies in different European countries
• Scientific writing and documentation expertise.

Qualifications

• Advanced degree in Life Sciences, Biomedical Engineering, or related field (PhD or MSc preferred).
• Minimum 10 years of experience in scientific affairs, clinical research, or medical affairs within IVD field
• Proven experience working with ethical committees and managing clinical studies at European level
• Fluent in English.

Location

• Thailand