My Volunteer Profile

Pharmaceutical professional with 15+ years of international experience in preclinical research, regulatory affairs, toxicity profiling, product safety, and scientific writing. SME for the neurosciences portfolio with a wide experience in multiple therapeutic areas (eg, neurology, diabetes, obesity, oncology, pain, and inflammation), where I abetted in simplifying complex data. Delivered editorial expertise in healthcare product development, journal manuscripts, review articles, posters, PPTs, and other educational material. Evaluated and prepared regulatory submissions related to efficacy and safety pharmacology sections. Experienced in filling IND applications.

Beside having strong verbal, written and interpersonal communication skills, I am skilled in the fields of publication planning, medical/scientific writing, project management, regulatory submissions, toxicology and, scientific reviewing/editing.

I am passionate about communicating scientific data/ideas clearly. My training in pharmaceutical sciences and biomedical research comes in handy, and the continuous learning from my colleagues and clients allows me to stay updated and perform efficiently.

Adroit at building lasting relationships with all my stakeholders, I am organized, adaptive, creative, self-motivated, energetic, result-oriented, and entrepreneurial in my work style. I combine critical thinking with unique client facing skills to best understand and solve key business problems.