Biodata |
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| Name of the Candidate | : | [Private] |
| Name of the Post Applied | : | Pharmacovigilance Executive |
| Job related skills / software | : | Identified potential product complaints, Established work priorities and directions independently with minimal input form Manager |
| Category | : | Medical |
| Sub Category | : | Pharmacovigilance |
| Years of Experience | : | 2 years |
| State | : | Maharashtra |
| Gender | : | Female |
| Salary Expected per Month(Rs) | : | 30,000 to 40,000 |
| Highest Qualification attained | : | B.Pharm. : Bachelor of Pharmacy |
| Major / Specialization | : | Pharma |
| Email Id | : | [Private] |
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| Are you looking for job now? | : | Yes |
| Can the recruiter contact you? | : | Yes |
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Pratima S Shirsat
E-Mail : pspratimashirsat002 AT gmail.com
Personal Details :
Date of Birth : 31-Mar-1993
Fathers Name : Siddharth M Shirsat
Nationality : Indian
Marital Status : Single
Languages Known : English,Hindi,Marathi
Hobbies : Reading novels,cooking.
OBJECTIVE :
Seeking a responsible and challenging position in a dynamic and stable workplace where I can enhance my professional skills and participate actively in the growth and development of the organization.
EDUCATIONAL QUALIFICATION :
** Bachelor of Pharmacy Yadavrao tasgaonkar institute of pharmacy, bhivpuri rd, Karja 2010– 2014
** HSC R.K.Talreja college of Arts,Commerce and Science 2008 – 2010
** Intermediate Guru nanak high school 2008
PROFESSIONAL EXPERIENCE :
Current working details :
Company details : TCS (Tata consultancy services), Vikhroli, Mumbai.
Designation : Process A
ssociate
Duration :Nov-2014-Present
WORK EXPERIENCE IN TCS Nov 2014-Present :
** Established work priorities and directions independently with minimal input form Manager.
** Identified potential product complaints.
** Remarkable knowledge to monitor and track Serious Adverse Events, serious and non-serious adverse drug reactions, and other medically related project information
** Identified case assessment related problems and reviewed reports
CIRRICULAR ACTIVITIES :
Actively participated in TCS purpose for life,social work activities and poster presentations on future impacts of clinical trial technologies.
ROLES AND RESPONSIBILITY :
** Case assessment, Duplicate check and case processing.
** MedDRA coding, WHO DD coding
** Narrative writing
** Expectedness or Listedness of adverse event
** Data entry in drug safety database
DOMAIN SKILLS :
** Adverse events and its reporting standards.
** Adverse events reporting forms.
DECLARATION :
I here by declare that the information furnished above is true to the best of my knowledge & confident enough to satiate your organization with outmost sincerity.
Date :
Place :
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