Biodata |
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| Name of the Candidate | : | [Private] |
| Name of the Post Applied | : | Pharmacovigilance Associate |
| Job related skills / software | : | Experience in case processing, product coding, event coding, narrative writing, MedDRA coding etc, Experience in databases like ARISG, Hands on experience of Clinical Trial cases, Allocation of cases as per seriousness and regulatory timelines. |
| Category | : | Medical |
| Sub Category | : | Pharmacovigilance |
| Years of Experience | : | 2 years |
| State | : | Andhra Pradesh |
| Gender | : | Female |
| Salary Expected per Month(Rs) | : | 40,000 to 50,000 |
| Highest Qualification attained | : | B.Pharm. : Bachelor of Pharmacy |
| Major / Specialization | : | Pharmacovigilance |
| Email Id | : | [Private] |
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| Are you looking for job now? | : | Yes |
| Can the recruiter contact you? | : | Yes |
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T.PADMAJA
Email : tpadmaja2611 AT gmail.com
CAREER OBJECTIVE :
To work in a competitive environment within a growing a organization that is conducive to personal growth and also make positive contribution to the organization.
PROJECT :
UV Spectrometric method development and validation for estimation of Dapsone.
ACADEMIC CREDENTIAL :
** B. Pharm St. Ann’s college of Pharmacy JNTUK 7.9 2021
** Intermediate Sri gowthami junior college Andhra Pradesh Board of Intermediate Education 7.98 2017
** S.S.C Sri sai high school Andhra Pradesh Secondary School Certificate 9.3 2015
PREVIOUS ORGANIZATION :
TATA CONSULTANCY SERVICES (Chennai)
DESIGNATION : Pharmacovigilance scientist 1
DURATION : From 11 Mar 2022 to 29 Aug 2023
EXPERIENCE & SKILLS :
** Experience in case processing, product coding, event coding, narrative writing, MedDRA coding etc.
** Experience in databases like ARISG.
** Hands on experience of Clinical Trial cases.
** Allocation of cases as per seriousness and regulatory timelines.
** Co-ordinate with Team Lead, Quality Reviewer, Medical Reviewer and Team Manager to ensure efficient reports solving.
** Planning, organizing, and managing daily work to meet service level timelines and deliverables.
** Working with the Safety Review team lead to escalate issues or tasks outside the normal scope of work.
** Assessing priority to cases i.e.
Immediate/High/Medium/Low using medical judgment.
** Encoding verbatim terms using MedDRA.
** Safety review of all type of cases including serious and non-serious study (clinical trial, NIP and spontaneous).
** Completing the adverse event case; and sending the updated and related documents or information to Medical Review Physician.
** Performing Quality checks and providing timely feedback.
** Performing daily responsibilities in accordance to all applicable Standard Operating Procedures (SOPs), conventions and client policies.
ACHIEVEMENTS AND EXTRA CURRICULAR ACTIVITIES :
** Presented power point presentation for Animal Pharmacology and Toxicological studies on the topic “Amoxapine, an antidepressant Pharmacology and Toxicology”.
** Presented power point presentation at Chalapathi institute of pharmaceutical sciences on the topic of Role of Pharmacovigilance on vaccine control.
PERSONAL DETAILS :
Name : Tiripathi Padmaja
Date of Birth : 11th Jun 2000
Marital Status : Single
Hobbies : Listening music, Cooking
Languages Known : Telugu & English
DECLARATION :
I solemnly declare that the statements made by me are true to the best of my knowledge and belief and I bear the responsibility for the correctness of the above-mentioned particulars.
DATE :
PLACE :
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