Ms. Chan's Professional Profile is as follows:
- 20 years experience in the life science industry
- Strong project management skills with 14 years direct experience in the discipline
- Certified in Project Management and Clinical Trials Design & Management
- Experience in managing all phases of a drug development program (Pre-Clinical, Clinical [Phase I,II
and III], and Post-NDA)]
- Experience managing Medical Device & Diagnostic projects toward market clearance and/or approval
- Experience managing Information Technology projects both in validated and non-validated
environments
- Knowledgeable in Good Laboratory Practices (GLP), Good Clinical Practices (GCP), and Good
Manufacturing Practices (GMP)
- Experience in the areas of Oxygen Therapeutics, Immunology, Respiratory Disorders, Cardiovascular
Imaging, Oncology, Hormone-related Disorders, Pharmacogenetics, Genomics, Histocompatibility
and Immunogenetics
- Excellent planning and facilitation skills; well organized, detail-oriented, and able to generate results to
achieve organizational objectives within time and budgetary expectations
- Dedicated team player; ability to communicate effectively with all organizational levels and functions
as well as external contractors and partners
