I have successfully completed 16 months, running a Clinical Trial Study in 24 centers all over India, for a German based Medical Device Organization (Translumina Therapeutics LLP).
The role allowed me to conduct all viable Clinical Research Initiatives. From Site feasibility check to Site initiation, Monitoring, and Ethics Committee regulations, I have ensured the smooth conduct of the study. Moreover, while my on-the-job experience has afforded me a well-rounded skill set, including first-rate communication and organization skills, I excel at:
• Project Management
• SAE reporting
• Site visits (Audits, motivational visits)
• Data Compilation
• Site evaluations
I have also gained extensive experience in legal and policy research, when formatting the Clinical Trial Agreements. However currently I’m conducting a role of a freelance medical writer. I have successfully designed protocol and case report forms, along with SOP’s for a medical device company and also delivered short articles for my company’s client doctors and their team. In the past I have been asked to revise the manuscripts that have now been published in renowned journals.
Moreover I have a sound background in science and medicine; hence I’m very flexible in writing about any related topic with thorough research. You can be assured about my writing style as it can be tailored according to my audience/clients demands and expectations.