Job Description:

• Design, conduct, and oversee laboratory experiments and clinical studies to investigate the causes, progression, and treatment of human diseases, disorders, and health conditions
• Collect, analyze, and interpret complex biological, chemical, and clinical data using statistical methods, bioinformatics tools, and specialized software to draw meaningful conclusions
• Participate in the discovery, development, and testing of new pharmaceuticals, medical devices, diagnostic tools, or therapeutic interventions
• Assist in the planning, implementation, monitoring, and evaluation of clinical trials, ensuring adherence to protocols, ethical standards, and regulatory requirements (e.g., FDA, EMA, ICH-GCP)
• Perform or supervise the processing and analysis of biological specimens (blood, tissue, fluids) using techniques such as cell culture, PCR, microscopy, flow cytometry, sequencing, and immunoassays
• Work closely with physicians, clinicians, biostatisticians, regulatory affairs teams, and cross-functional research groups to translate findings into actionable medical insights
• Prepare detailed technical reports, research papers, grant proposals, and presentations for scientific journals, conferences, and internal stakeholders
• Ensure all research activities comply with institutional, ethical (IRB), biosafety, and regulatory guidelines; maintain accurate documentation and laboratory records
• Work with junior scientists, research associates, and laboratory technicians; maintain laboratory equipment and supplies
• Collaborating with technology inventors and clinical trial organizations to apply new inventions in clinical settings
• Initiating and executing investigator-initiated trials and sponsored trials to study, validate and improve novel products and services for clinical use
• Translating research outcomes into marketable applications and business opportunities
• Delivering high-quality presentations to collaborators and partners
• Handling other relevant tasks as assigned by the supervisor(s)

Requirements

• MD / PhD / MBChB in Medicine and Surgery, Chemical Pathology, Medical Science, Clinical Medicine, Public Health, Biostatistics, or related medical disciplines
• 10+ years of solid work experience in Hospital Authority setting
• Hands-on skills on molecular diagnostics, cfDNA and translational assay development
• Track record of leadership and project management in IVD R&D, including NGS and biomarker validation
• Experience in cross-functional collaboration with bioinformatics and clinical teams is a definite advantage
• Mature, self-motivated, and able to work under pressure
• Highly proficient and fluent in English in both writing and verbal communications

A highly competitive salary commensurate with qualifications and experience will be offered, in addition to annual leave and medical benefits.

Applicants should submit their up-to-date C.V., quoting the job reference number, with information on current/expected remuneration and availability, to hr@abic.hk. Review of applications will commence as soon as possible and until the posts are filled.

Job Description:

• Design, conduct, and oversee laboratory experiments and clinical studies to investigate the causes, progression, and treatment of human diseases, disorders, and health conditions
• Collect, analyze, and interpret complex biological, chemical, and clinical data using statistical methods, bioinformatics tools, and specialized software to draw meaningful conclusions
• Participate in the discovery, development, and testing of new pharmaceuticals, medical devices, diagnostic tools, or therapeutic interventions
• Assist in the planning, implementation, monitoring, and evaluation of clinical trials, ensuring adherence to protocols, ethical standards, and regulatory requirements (e.g., FDA, EMA, ICH-GCP)
• Perform or supervise the processing and analysis of biological specimens (blood, tissue, fluids) using techniques such as cell culture, PCR, microscopy, flow cytometry, sequencing, and immunoassays
• Work closely with physicians, clinicians, biostatisticians, regulatory affairs teams, and cross-functional research groups to translate findings into actionable medical insights
• Prepare detailed technical reports, research papers, grant proposals, and presentations for scientific journals, conferences, and internal stakeholders
• Ensure all research activities comply with institutional, ethical (IRB), biosafety, and regulatory guidelines; maintain accurate documentation and laboratory records
• Work with junior scientists, research associates, and laboratory technicians; maintain laboratory equipment and supplies
• Collaborating with technology inventors and clinical trial organizations to apply new inventions in clinical settings
• Initiating and executing investigator-initiated trials and sponsored trials to study, validate and improve novel products and services for clinical use
• Translating research outcomes into marketable applications and business opportunities
• Delivering high-quality presentations to collaborators and partners
• Handling other relevant tasks as assigned by the supervisor(s)

Requirements

• MD / PhD / MBChB in Medicine and Surgery, Chemical Pathology, Medical Science, Clinical Medicine, Public Health, Biostatistics, or related medical disciplines
• 10+ years of solid work experience in Hospital Authority setting
• Hands-on skills on molecular diagnostics, cfDNA and translational assay development
• Track record of leadership and project management in IVD R&D, including NGS and biomarker validation
• Experience in cross-functional collaboration with bioinformatics and clinical teams is a definite advantage
• Mature, self-motivated, and able to work under pressure
• Highly proficient and fluent in English in both writing and verbal communications

A highly competitive salary commensurate with qualifications and experience will be offered, in addition to annual leave and medical benefits.

Applicants should submit their up-to-date C.V., quoting the job reference number, with information on current/expected remuneration and availability, to hr@abic.hk. Review of applications will commence as soon as possible and until the posts are filled.