Profile
I am a professional with specialization in Biotechnology, having cross-functional experience as a Lead scientific researcher, Mentor, Trainer, writer and Pat-informatics professional. I bring with me over 8.2 years of cumulative experience in Secondary research, scientific or publication writing, clinical research and development, data analysis/data interpretation and team management.
Experience in Intellectual Property Management (Patents-Life-science, Healthcare, biological sciences) writing, editing, fact checking, drafting and reviewing published scientific literature and guidance documents and QC documents.
Actively involved with research teams to accurately and appropriately capture and record data for scientific study and validation.
Handled independent project which involved patent assessment, and competitive and comparative analysis of the product.
In addition, have gained diverse cross-functional experience in Clinical trials process, Clinical Drug Discovery and Clinical trial editorial operations.
On the whole, providing an upright and readily available intelligent information and subject matter expertise to assist the highly competitive Pharmaceutical and healthcare industries and organizations.
Currently as a tenured Analyst, Quality Co-ordinator and Subject Matter Expert, I am responsible for the overall Quality and productivity output of the team.