Friday, December 20, 2019

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


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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