
PROFESSIONAL SUMMARY:
Looking for a challenging role in a reputable organisation to utilize my skills and knowledge for the growth of the organisation as well as to enhance my knowledge about new and emerging trends.
As a drug safety associate, I have involved in Numerous work responsibilities. Like adverse event monitoring, Case processing of different type of case reports and executive the Validity assessment and quality of the reports and sending it to Regulatory authority of country.
Keeping a check on all applicable Regulations and Stranded operating procedures (SOPS). And analyzing the date received from clinical Reports and submitting it to the regulatory authority. Coordinating and conducting knowledge sharing sessions and Discussion about different case .Scenarios in the team. And working with different types of tools to improve the patient Outcomes.
Certified in " Introduction to Drug Safety and Pharmacovigilance an Abridged Course " by Biopharma Institute in December 2020.
Certified in " Good Clinical Practice " by NIDA Clinical Trials Network in December 2020.
Certified in “Introduction to Clinical Research” from The Global Health Network in November 2020.