eSupervisor Detail

About me

PhD-qualified biotechnologist with experience in oncology, nanobioscience, and proposal development. Worked at LabCorp Drug Development, supporting assay development and oncology proposals. Core competencies: Oncology, Proposal writing, Clinical research, Literature search, Regulatory compliance, Drug-related studies, Scientific writing, Clinical Trial Operations (Foundational), ICH-GCP Compliance, Study Documentation, SOP Adherence, RFI/RFQ/COMS experience, and CTMS & eTMF Familiarity

Interests: Life sciences professional with a PhD in Biotechnology and 3+ years of industry experience at Labcorp Drug Development supporting oncology research services and proposal strategy. Experienced in translating complex scientific study designs into commercially viable proposals, collaborating with cross-functional stakeholders, and supporting business development activities in a CRO environment. Strong foundation in preclinical oncology research, clinical trial processes, and regulatory frameworks. Interested in leveraging scientific expertise, market understanding, and emerging digital health technologies to support strategic decision-making and innovation in the life sciences industry.