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Bioclinica India - Walk-In Drive for Pharmacy, Dental, Nursing Freshers on 21st December 2019
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