I am a trained molecular biologist with expertise in oncology, wound care, and fluorescence imaging. I specialize in managing clinical trials, developing educational materials, and presenting scientific research to global audiences. My experience includes leading cross-departmental collaborations in clinical trials, product development, and medical affairs, as well as designing and executing preclinical and in vitro studies.

I offer services in molecular biology techniques, clinical education, and scientific communication. My technical expertise includes bacterial fluorescence imaging, cell culture, qRT-PCR, cloning, immunoblotting,…

I am a regulatory affairs professional with 3 years of experience contributing to drug development and ensuring regulatory compliance across the product lifecycle. My expertise includes preparing and submitting regulatory documents such as INDs, IMPDs, CTAs, NDSs, S(NDS)s, NDAs, and MAAs, with proficiency in CMC documentation, eCTD submissions, and regulatory timeline management. I have supported successful approvals and compliance with Health Canada, FDA, and EMA standards.

I specialize in regulatory strategy, regulatory operations, labeling, and change control assessments, as well…