Monday, January 6, 2020

Freshers Walk-in @ Bioclinica Bangalore on 19th Jan 2020 for Voice Process


Freshers Walk-in @ Bioclinica Bangalore on 19th Jan 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: 19th Jan 2020 (Sunday)

Job Title: Drug Safety Associate – MICC

Years of experience: Freshers

Work Location: Mysore, Karnataka

Shift Timings: US shift (With cab facility)

Education: Graduates / Post Graduates in Pharmacy, Nursing, Dental or any equivalent

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

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

Communication Skills:

Excellent written/oral communication

Strong interpersonal skills required to interact with clients, management, and peers effectively.



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