Wednesday 15 August 2018
BIOCLINICA - Walk-In Interviews for Freshers & Experienced Candidates on 18th August, 2018
Pharma Wisdom Jobs
20:15:00
3
**Candidates who are attending this drive should be registered or applied for the state council registration
Meet us on Saturday, 18th August between 9 AM to 1 PM at the below address:
Bioclinica India Pvt. Ltd
No:18/2 & 18/3, V G Heritage,
Vanivilas Road, Kanakapura,
Basavanagudi, Bengaluru,
Karnataka 560004
Job Title: Drug Safety Associate
Work Location: Mysore
Years Of Experience: 0 to 2 Years
Educational Qualification: B Pharmacy, M Pharmacy, Pharm D, BDS, MDS, BAMS, BHMS, B.Sc Nursing, M.Sc Nursing
ROLES & RESPONSIBILITIES
As Case Intake Member:
- Responsible for case intake, duplicate check, and registration
- Maintain log of source documents and other communications
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.
As Literature Review Specialist
- Ensure effective and accurate collection, recording, review and reporting of literature searches conducted.
- Review of literature articles to identify case safety reports.
- Responsible for operational Pharmacovigilance activities for assigned developmental and /or marketed products.
- Assist in signal generation and safety analysis activities.
- Ensure quality of literature searches and reporting.
- Review of local/global literature reports to determine regional reportability.
- Create/maintain study summary documents.
- Assist with narrative writing for periodic/ad hoc submissions.
- Assist with ad hoc or routine safety monitoring activities.
Job Title: Drug Safety Associate
Work Location: Mysore
Years Of Experience: 0 to 2 Years
Educational Qualification: B Pharmacy, M Pharmacy, Pharm D, BDS, MDS, BAMS, BHMS, B.Sc Nursing, M.Sc Nursing
ROLES & RESPONSIBILITIES
As Case Intake Member:
- Responsible for case intake, duplicate check, and registration
- Maintain log of source documents and other communications
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.
As Literature Review Specialist
- Ensure effective and accurate collection, recording, review and reporting of literature searches conducted.
- Review of literature articles to identify case safety reports.
- Responsible for operational Pharmacovigilance activities for assigned developmental and /or marketed products.
- Assist in signal generation and safety analysis activities.
- Ensure quality of literature searches and reporting.
- Review of local/global literature reports to determine regional reportability.
- Create/maintain study summary documents.
- Assist with narrative writing for periodic/ad hoc submissions.
- Assist with ad hoc or routine safety monitoring activities.
