New job Safety Writer-Aggregate Reporting(AR) in Telangana

Safety Writer-Aggregate Reporting(AR)

Company : Novartis HQ
Salary : Details not provided
Location : Telangana

Full Description

Novartis HQ

Safety Writer-Aggregate Reporting(AR)

Hyderabad
Full time

Industry
Pharmaceuticals
Date posted
May 13, 2021
Starting Date
May 12, 2021
Preferred Skills
Adaptablility
Verbal Communication
Written Communication
Time Management
Multi-tasking
Working Under Pressure
Leadership
Problem-solving
Teamwork
Field of Education

Business & Management Studies

Level of Education

Bachelors

Novartis HQ

Novartis International AG is a Swiss multinational pharmaceutical company based in Basel, Switzerland. It is one of the largest pharmaceutical companies in the world.

What you’ll do
• Monitors and audits the company’s drug, biologics or medical devices surveillance program including the intake, evaluation, processing, and follow-up on adverse reports. Participates in the resolution of any legal liability and in complying with government regulations. • Ensures accurate receipt, maintenance, and assessment against product labeling. Reports events or reactions as required by regulatory agencies including adverse events data from clinical trials, spontaneous or solicited sources, periodic and experience reports. May provide trending and safety signal detection and assessment. Supports all clinical trial activity and post marketing. • To support management of operational processes in ensuring compliance with Novartis global/local procedures, national and international regulations/standards/guidelines for pharmacovigilance of Novartis marketed and investigational products • Manage collection, processing, documentation, reporting and follow-up of all adverse events (AE) reports for all Novartis products from clinical trials, post-marketing studies (PMS), Patient Oriented Programs (POP), registries and all Spontaneous Reports (SR). • Transcribe, translate (where required) and enter data of all Serious Adverse Events (from Clinical Trials,) and all adverse events (from POPs, PMS, registries and all SRs) from source documents onto safety systems accurately and consistently with emphasis on timeliness and quality. • Record and track receipts, submissions and distributions of documents like SAEs, SRs, Investigator Notifications etc in cooperation with other departments -Manage reporting/submission/distribution of safety reports/updates/information to Local Health Authorities and/or clinical operations in cooperation with other Departments. Work with other local/global PV associates to ensure accurate evaluation of safety data. • Interact and exchange relevant safety information with LHA, PV associates, other functional groups, and third-party contractor, if applicable. -Survey and monitor global/ regional/national (as applicable) pharmacovigilance regulations and provide update to global PVO organization. -Develop, update, and implement local procedures to ensure compliance with PVO global procedures and national requirements. -Management and maintenance all relevant assigned PVO databases, if applicable. • Develop and update training materials for pharmacovigilance. Ensure support for and close-out of audits, corrective action plan activities and Health Authority inspections. Provide timely, relevant information to trial coordinators, CRAs and other Novartis staff
What we're looking for
• Operations Management and Execution • Collaborating across boundaries Functional Breadth • Global Regulatory compliance to world-wide Health Authorities and external partners for AR Quality of support to health authority inspections and audits

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