Bioclinica Walk-in Pharmacy / Dental / Nursing Freshers on 21st Dec 2019
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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