Daksha Gupta Email & Phone Number

United States

India

Advising and helping students in presenting papers, communication and personality development via international conferences platform.Giving feedbacks in order to help the organization and students to be better.Helping in making and organizing schedules of meetings and presentations.

Bengaluru, Karnataka, India

Data entry including creating case, checking duplicity and confirming case validity into safety database Argus.Quality reviewed and processed adverse event reports (spontaneous, solicited, literature and license party cases) of drugs from Pfizer and Novartis.Triaged case reports based on the seriousness of the adverse events.Coded suspect drugs, concomitant medications, patient’s medical history and adverse events using WHO drug dictionary and MedDRA.Involved in a thorough and accurate clinical narrative writing and editing as per the regulatory guidelines.Assessed laboratory test results and generated action items for sending follow up questionnaires.Determined causality of adverse events with the help of medical reviewers.Submitted case reports to health authorities following the case submission timelines.Worked on myriad therapeutic areas including rheumatology, cardiovascular, neuroscience. Also processed reports on over the counter products.Developed and maintained expertise and knowledge of all assigned products within a therapeutic area, applicable corporate and global regulations, guidelines, Standard Operating Procedures and writing practices, data entry conventions, and search functions in the safety database.Aided management in achieving common goals like meeting regulatory submission timelines and finishing trainings before time.Received client appreciation for case quality.

Mumbai, Maharashtra, India

Received and accurately documented Adverse Events (AE), Product Complaints (PC) and Medical Inquiries (MI) from patients and Health Care Professionals (HCPs) in compliance with company policy.Provided medical input for queries regarding the drugs/products from Pfizer and their documentation using standard operating procedure to HCPs and consumer.Identified and captured any adverse events related to the drugs of therapeutic areas including cardiovascular and metabolic with over the counter medications.Did classification of the safety data using MedDRA knowledge.Documented product related complaints for the drugs and medical devices.Provided information regarding drugs to health care professionals.Documented the AE on a safety report form (CRF's), performed a quality check and subsequent submission to the client following regulatory timelines.Used global software Argus for processing cases.Performed a triage on the reports to identify seriousness.Part of the Audit team in 2013.Received appreciation from client (Pfizer) and supervisors for quality in cases.

Hyderabad, Telangana, India

• Performed secondary research on pipeline products.• Paraphrased and reconstructed available data and entered into database using specific tools • Managed and tracked time frames to meet deadlines.

M. Pharma., Pharmacognosy, 3.57 Gpa

Post Graduate Diploma, Preventive And Promotive Healthcare (Pphc), 2.7 Gpa

Bachelor Of Pharmacy (B.Pharm.), Pharmacy, 3.49 Gpa