Summary
Overview
Work History
Education
Skills
Additional Information
Languages
Personal Information
Timeline
Hi, I’m

ADIL PARVEZ

New Delhi

Summary

Evaluates consistency, Pharmacovigilance Performed roles of Triage, Case Processor, Narrative Writer. Case processing experience of 'Spontaneous and "NonInterventional Study' (including Literature)'report types including 'Regulatory', 'Licensee', 'Affiliate' and Clinical trial cases. Review the cases, identify the correction required in the case and segregate them based on minor case correction (MCC) and significant case correction. raising query related to the required protocol numbers and get them configured into the system. Assess the need for follow up infor Familiar with processing of NALP, Literature and LOE, AT Risk, Invalid, Internet Source, scenarios. MedDRA (Medical Dictionary for Regulatory Activities) code for each adverse event and accuracy of product label assessments for each adverse event. Working on database ARGUS and Pfoenix for comparison of Adverse Events and completing follow-up.

Overview

11
years of professional experience

Work History

Qinecsa

Senior Drug Safety Associate
04.2021 - 01.2024

Job overview

  • Argus safty ICSR, Evaluates consistency, completeness, accuracy of safety database (ARGUS), tracking database and source document entry forms Be responsible in meeting timelines, and quality standards
  • Reporting on daily basis internally to service delivery leader regarding case status (In training ) Submission of the cases to the POCs for review on daily basis (In training) ??
  • Updating the case tracker and forwarding to Service delivery leader for review
  • Collating the monthly data regarding the cases status ??
  • Mentoring of associates on day to day basis ??
  • Sharing the client updates to the team ??
  • Preparing Monthly Stacks forthe Associates & QC as per their performance
  • Responsible for preparation and updating of SOPs as per Client's convention
  • Review of source documents such as physician office records, hospital records and lab details for the cases received from legal/and their agents ??
  • Completion of the data entry from source docs including a narrative, complete the custodial review, detailing the adverse events, selection and coding of event terms, concomitant medications and medical history against source docs ??
  • Undergo client mentorship as designated by the project manager PSSR, literature review, case processing, Team Management of 20 employees with there performance training, daily meetings with team about there issues. Client meetings for quality and error with there resolution. Quality improvement plans implementation.

wipro Bps

Pharmacovigilance Officer (Quality Reviewer)
04.2017 - 04.2021

Job overview

  • Completion of the data from source docs including a narrative (narrative writing), complete detailing the adverse events, selection of event terms, concomitant medications and medical history against source docs
  • Working on database Pfoenix and ARGUS for comparison of Adverse Events and completing follow-up reports
  • MedDRA (Medical Dictionary for Regulatory Activities) code for each adverse event and accuracy of product label assessments for each adverse event
  • Familiar with processing of NALP, Literature and LOE, AT Risk, Invalid, Internet Source scenarios
  • Working on litrature cases.process associate

Wipro BPS

Pharmacovigilance Officer (Data Entry)
04.2015 - 04.2017

Job overview

  • Pharmacovigilance Familiar with processing of NALP, Literature and LOE, AT Risk, Invalid, Internet Source, scenarios
  • MedDRA (Medical Dictionary for Regulatory Activities) code for each adverse event and accuracy of product label assessments for each adverse event
  • Working on database ARGUS and Pfoenix for comparison of Adverse Events and completing follow-up reports
  • Preparation and review/update
  • Participated in the preparation of training materials
  • Team lead activitie, case tracking, quality meeting with client.

Genpact

Officer
06.2013 - 05.2014

Education

Uttar Pradesh Technical University (UPTU)

M.Pharma - Pharmacy
01.2012

Uttar Pradesh Technical University (UPTU)

B.Pharma - Pharmacy
01.2010

Skills

  • Registered Pharmacist
  • Pharmacist
  • Team managements
  • Quality assurance

Additional Information

9 Years 0 Month

Languages

English
Hindi
Urdu

Personal Information

Title: SENIOR DRUG SAFETY ASSOCIATE

Timeline

Senior Drug Safety Associate

Qinecsa
04.2021 - 01.2024

Pharmacovigilance Officer (Quality Reviewer)

wipro Bps
04.2017 - 04.2021

Pharmacovigilance Officer (Data Entry)

Wipro BPS
04.2015 - 04.2017

Officer

Genpact
06.2013 - 05.2014

Uttar Pradesh Technical University (UPTU)

M.Pharma - Pharmacy

Uttar Pradesh Technical University (UPTU)

B.Pharma - Pharmacy
ADIL PARVEZ