I feel confident in my ability to tackle any challenge and feel strongly that there is a ‘solution’ to every obstacle

I’m a Drug Safety Consultant/Regulatory Medical Writer with over 7.5 years of experience in clinical research industry. I have proven abilities in the field of Pharmacovigilance Management and I've developed a breadth of skills through my work in Pharmacovigilance, Clinical research, Medical coding, Clinical Data management, Medical review, and Training of team members.
I have worked in multiple therapeutic areas such as Oncology, Infections and Infestations, Dermatology, Cardiovascular, Rheumatology, Immunology/Autoimmune Diseases, Metabolic disorders, Hematology, Virology and Psychiatric and CNS Disorders. I have authored reports for vaccines and medical devices too.
I had an opportunity to explore my knowledge in different buckets of the processes and have handled key roles and responsibilities.
With excellent oral and written communication, I had been conducting and communicating with the clients.
My goal is to make use of my experience and skills to make impactful business decisions and work in pragmatic way so that I can grow professionally and personally with full integrity, hard work and prove to be a sagacious performer.

Work Terms

Working hours: Can work for 8 hours/day and 40 hours per week but I'm quite flexible with working hours..!! Can extend depending upon the work and its turn-around time..!!
Mode of Communication: Would prefer communicating on mail or any communicator or phone or whatsapp
Mode of Payment: Paypal