Bioclinica Pharmacovigilance (Drug Safety Associate) Job openings for Pharmacy Candidates 2022

Bioclinica (Clario) currently hiring for Experienced Drug Safety professionals, IMMEDIATE – 30 Days”

Work Location: Mysore, Karnataka

Essential Duties and Responsibilities:

As Quality Check Reviewer

  • Review data entered in safety database for completeness and accuracy.
  • Provide quality feedback to team resources
  • Track and maintain quality metrics

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.

Working Conditions: Normal office environment.

Hours: Standard Hours 40 hours per week, one hour lunch, Monday – Friday. Additional hours as needed.


Other responsibilities:

  • Following up with sites regarding outstanding queries.
  • Follow up on reconciliation of discrepancies.
  • Follow departmental AE workflow procedures.
  • Closure and deletion of cases.
  • Mentor and guide the activities of the Dug Safety Associate.
  • High level of proficiency al all workflow tasks.
  • Perform any other drug safety related activities as 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.

Experience: 1 – 3 Years in Pharmacovigilance

Education: Any Registered Healthcare Professionals (B Pharm / M Pharm / Pharm D)


If your profile is suitable and interested kindly share your resume to Nithin.vijendra@bioclinica.com / roopa.shree@bioclinica.com / sscrazybuddy@gmail.com

Note: Please mention your notice period in subject line

Please note due to High Volume of applications being received, only the relevant profiles for this post will receive a response. Thank you for understanding.

Bioclinica Pharmacovigilance (Drug Safety Associate) Job openings for Pharmacy Candidates 2022
Bioclinica Pharmacovigilance (Drug Safety Associate) Job openings for Pharmacy Candidates 2022

1 thought on “Bioclinica Pharmacovigilance (Drug Safety Associate) Job openings for Pharmacy Candidates 2022”

Leave a Reply

Scroll to Top
%d bloggers like this: