Pharmacy / Dental / Nursing Freshers Walk-in
@ Bioclinica on 21st Dec
Greetings from Bioclinica..!!
As part of our expansion process, we are
conducting Freshers (2017/18/19 ) walk-In at our
Mysore Campus.
Walk In Venue:
Bioclinica India Pvt. Ltd, Abbhi Campus,
Belagola Industrial Area, Metagalli (Village), Mysore, Karnataka
Walk-In Timings: from 9.30 AM to 12 PM
Walk-In Date: 21st Dec 2019 (Saturday)
Please go through the below job description .
Job Title: Junior Drug Safety Associate
Work Location: Mysore, Karnataka
Primary 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.
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
Secondary Responsibilities
·
Basic competence with medical and therapeutic terminology
·
Understanding of Patient Safety regulatory obligation
·
Good attention to detail
·
Ability to deliver within established timelines
·
Fluency in Spoken and written English and excellent comprehension
Qualifications:
Education : Any
healthcare professionals (B Pharm / M Pharm / Pharm D / BDS / BSc Nursing)
Experience : 0-1 year
of experience in pharmacovigilance
Additional Skills:
·
Strong motivational skills and abilities, promoting a team-based
approach
·
Strong interpersonal and communication skills, both verbal and
written
·
Strong organizational and leadership skills
·
Goal-oriented
·
Ability to maintain professional and positive attitude
Working conditions
Travel: 0-50% (can be adjusted)
Lifting: 0-50 lbs. (can be adjusted)
Other: Computer work for long periods of
time
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