WALK IN – B Pharmacy, M Pharmacy, Pharm D, BAMS, BHMS ON 3rd March

WALK IN – B Pharmacy, M Pharmacy, Pharm D, BAMS, BHMS ON 3rd March  

PV Chronicle shares one more Walk in interview information WALK IN – B Pharmacy, M Pharmacy, Pharm D, BAMS, BHMS ON 3rd March. Please find the details below.

Time and Venue

 3rd March, 9 AM onwards

Bioclinica #18/2, Vani Vilas Road,

Basavanagudi, Bangalore – 560 004.

Landmark: Near Lalbagh Botanical Gardens, Opposite Sree Sudarshana Vidya Mandir

JOB TITLE: Drug Safety Associate
WORK LOCATION: Mysore
YEARS OF EXPERIENCE: 0 to 2 years
EDUCATION: B PHARMACY, M PHARMACY, PHARM D, BDS, MDS, BSC NURSING, MSC NURSING, BAMS, BHMS
ESSENTIAL DUTIES AND RESPONSIBILITIES: 

As Case Intake Member: 

  • Responsible for case intake, duplicate check, and registration
  • Maintain log of source documents and other communications

As Case Processor:

  • Responsible for data entry of individual case safety reports into the safety database.
  • Review and evaluate AE case information to determine required action based on and following internal policies and procedures
  • Process all incoming cases in order to meet timelines
  • Full data entry including medical coding and safety narrative

As Medical Coder 

  • Responsible for coding all medical history, events, drugs /procedures/indications and laboratory tests according to the appropriate dictionary (For e.g. MedDRA, Company Product Dictionary, WHO-DD)

As Narrative Writer

  • Responsible for writing medically relevant safety narrative of cases and checking the completeness and accuracy of the data entered in the various fields.

As Literature Review Specialist

  • Ensure effective and accurate collection, recording, review, and reporting of literature searches conducted.
  • Review of literature articles to identify case safety reports.
  • Responsible for operational Pharmacovigilance activities for assigned developmental and/or marketed products.
  • Assist in signal generation and safety analysis activities.
  • Ensure quality of literature searches and reporting.
  • Review of local/global literature reports determining regional reportability.
  • Create/maintain study summary documents.
  • Assist with narrative writing for periodic/ad hoc submissions.
  • Assist with ad hoc or routine safety monitoring activities.

OTHER RESPONSIBILITIES:

  • Following up on sites regarding outstanding queries.
  • Follow up on reconciliation of discrepancies.
  • Follow departmental AE workflow procedures
  • Closure and deletion of cases
  • Perform any other drug safety-related activities as assigned
  • Perform literature review activities when trained and assigned.

SPECIALIZED KNOWLEDGE AND SKILLS:

  • Basic competence with medical and therapeutic terminology.
  • Ability to work independently but guided by documented procedures, with appropriate support.
  • Able to work effectively as part of a team.
  • Understanding of patient safety regulatory obligations.
  • Should be familiar with regulatory & pharmacovigilance guidelines.
  • Should be familiar with pharmacovigilance terminology.
  • Excellent attention to detail.
  • Ability to deliver within established timelines.
  • Fluency in English and excellent comprehension.
  • Computer literate.
  • Relevant product and industry knowledge.
  • Experience with relevant software applications.

Source: Naukri

Do not miss to share WALK IN – B Pharmacy, M Pharmacy, Pharm D, BAMS, BHMS ON 3rd March on your social connections including Whatsapp, Facebook, and LinkedIn. Feed us in comment box for better writing.

Leave a Reply

Your email address will not be published. Required fields are marked *