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 [email protected] / [email protected] / [email protected]
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.
