Biomedical Research Professional
2 weeks ago
Job Summary
We are seeking a skilled Clinical Scientist to join our team at Advanced Biomedical Instrumentation Centre Limited. As a key member of our team, you will be responsible for leading clinical development projects and collaborating with technology inventors and clinical trial organizations.
Key Responsibilities
- Developing clinical protocols with professors, collaborators, clinical KOLs, and industry partners
- Managing regulatory and clinical development matters relating to IRB, GCP, GLP, ICH guidelines, HIPAA governance, US FDA, China NMPA, EMA, Japan PMDA, IVD-R, IND, etc.
- Initiating and executing investigator-initiated trials and sponsored trials to study, validate and improve novel products and services for clinical use
- Coordinating research projects, executing experiments, solving technical challenges, and achieving desirable project results
- Translating research outcomes into marketable applications and business opportunities
- Writing proposals, reports, articles, patents, technical specifications, and other publications
- Delivering high-quality presentations to collaborators and partners
- Handling other relevant tasks as assigned by the supervisor(s)
Requirements
- M.D./M.B.B.S./M.B.Ch.B./Ph.D./M. Phil./M.Sc./M.Phil./B. Pharma degree in Medical Science, Clinical Medicine, Public Health, Biostatistics, or related medical disciplines
- Knowledge in both medical laboratory and clinical trials 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
- Relevant industry experience in the healthcare/biotech sector is a MUST: 1+ year of experience after obtaining PhD degree (registered medical doctor licence is considered equivalent to PhD); or 2+ years of experience after obtaining master degree
- Relevant industry expertise in specialized areas such as Animal or Human Neurosurgery, Neurophysiology, or Neuropathology, Cancer diagnostics and treatment, Contract Development and Manufacturing Organization (CDMO) for Pharmaceuticals, FDA-Related Regulatory Affairs, Fertility and Reproductive Medicine Laboratory, Interventional Cardiology or Interventional Radiology, Multi-Cancer Early Detection (MECD), Ophthalmology Medical Devices, Organoids, Orthopedic Implants, Point-of-Care Testing (POCT) Devices for Pathogens or Chronic Diseases, Respiratory Drug Formulation Development
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