BIOCLINICA - Walk-In Interviews for FRESHERS on 15th & 16th Feb' 2020

Walk-In @ Bioclinica Bangalore on 15th & 16th Feb for Voice Process

Greetings from Bioclinica..!!

As part of our expansion process, we are conducting Freshers Walk-In at our Bangalore Campus.

Walk In Venue:

Bioclinica India Pvt Ltd,

No:18/2 & 18/3, V G Heritage,

Vanivilas Road, Kanakapura,

Basavanagudi, Bengaluru,

Karnataka 560004

Walk-In Timings : from 9.00 AM to 1 PM

Walk-In Date: 15th and 16th Feb 2020

Job Title : Drug Safety Associate - MICC
Years of experience: Freshers
Work Location: Mysore, Karnataka
Shift Timings: US shift (With cab facility)
Education: Bachelor's / Master's in Science / Nursing / Bio-Informatics / Biochemistry / Biomedical / Biotechnology / Clinical Microbiology / Medical Biotechnology / Biological Science / Biomedical Sciences / Biosciences /Life Sciences / Medical Biochemistry / Medical Microbiology / Molecular Biology / Life Sciences / Clinical Research / Biophysics / Medicinal Chemistry / Nuclear Sciences
Essential Duties and Responsibilities:

· Receive and process assigned voicemails

· Update the Voicemail Tracker

· Receive information or inquiry through phone call/email/fax/mail and create a record in Track Wise and IRMS

· Attach product replacement authorization form in Track Wise, if inquiry involves replacement request

· Follow Track Wise Convention guide while handling and managing product complaints.

· Receive information or inquiry through phone call/email/fax/mail and process them in IRMS

· Generate reports related to inquiries received through phone call/email/fax/mail

· Enter all the relevant information received through phone calls/email/fax/mail into IRMS

· Enter all the information pertaining to non-significant phone caIIs, emails, faxes for internal tracking and reconciliation

· Responsible for receiving phone calls related to adverse events and for book-in of cases received by all source types (phone call/email/fax/mail) into ARIS-g

· Responsible for following good documentation practices while completing AEM form

· Responsible for triaging of case

· Responsible for attaching AEM form or other source documentation to case.

· Use IRMS to create contacts for callers with inquiries related to AE/PC/MI.

· Thorough understanding of use of FAQs and product labeling to answer medical information inquiries

· Thorough understanding of regulatory requirements for safety reporting

Other Responsibilities:

· Follow departmental AE workflow procedures

· Closure and deletion of Cases

· Perform any other drug safety related activities as assigned

Specialized Knowledge and Skills:

· Basic competence with medical and therapeutic terminology