I am a seasoned professional with extensive experience in research work and medical writing, handled many complex projects and executed them effectively. Highly committed, dedicated individu

Leveraging my project management skills developed through extensive academic experience and coursework projects, along with my strong writing abilities, I am well-suited for a project coordinator, assistant or medical writer role in pharmacovigilance. Throughout my academic career, I have successfully managed multiple research projects, coordinating tasks, timelines, and resources to ensure project completion and compliance with regulatory standards. My coursework projects have further refined my ability to handle complex data, collaborate with cross-functional teams, and produce detailed reports.

In addition to project management, my role as an Assistant Professor has significantly enhanced my writing skills. I have authored numerous research papers and awarded, all requiring clarity, precision, and attention to detail. My experience in medical writing has particularly honed my ability to translate complex scientific information into clear, accessible documents. This skill is crucial in pharmacovigilance for accurately documenting adverse events, preparing regulatory submissions, and communicating findings to diverse stakeholders.

Skills Sets:-
Pharmacovigilance Operations: Hands-on experience in Argus Drug Safety Software.Proficient in the literature review, adverse event data collection, processing, management and reporting,
Project management:-Mindmap, Gantt Chart(experience in Gantter task management and project planning software).

Along with my profession, I love travelling to serene and spiritual places because of my inclination towards living close to nature and meeting different people with different cultures and beliefs.

Work Terms

I can Spend 2 hrs every day finishing up my project and I will charge 4$ per hour. My way of communication is my Gmail Id shiprapharma87@gmail.com

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