223 Shares 1962 Views

Drug Safety Associate – Novo Nordisk – Location Bangalore, IN

Jun 13, 2017
223 Shares 1,962 Views

Job description

Novo Nordisk is one of the world’s most successful pharmaceutical companies with a great growth potential. Do you want to be part of this?Safety Operations Bangalore is part of Global Safety who has the global responsibility for surveillance of the Safety and Quality of Novo Nordisk clinical development and marketed products. Safety Operations Bangalore is responsible for global handling and reporting of adverse event reports.

Position DescriptionAs a Drug Safety Associate you will be part of a young and dynamic team currently consisting of 72 dedicated employees.Responsibilities includePerform initial evaluation of reported adverse events (serious and non-serious) from all sources.

  • Perform case entry and verification of reported non-serious and serious adverse events; enter the reported information in the Novo Nordisk safety database, on the basis of individual case histories, correspondence with affiliates/sites and other departments in headquarters (HQ) and various administrative assignments.
  • Ensure accurate and consistent coding of all events for serious and non-serious cases entered in the Argus with the use of MedDRA (Medical Dictionary for Regulatory Activities).
  • Evaluate causality, seriousness and listedness for all cases.
  • Ensure that case narrative comprises correct and appropriate safety information.
  • Assess the need for follow up information and issue follow up requests for all cases and post queries in EDC and/or to affiliate
  • To be responsible for Periodic Safety Update Report (PSUR) clean up and other case clean-up activities.
  • Ensure that all tasks are performed in compliance in accordance to GXP requirements.
  • Maintain a network of safety contacts within Global Safety (GS) and affiliates.
  • Participate in projects in Global Safety or in other parts of the organisation with impact in Global Safety processes.
  • Liaise with affiliates and partners for local literature and compliance.
  • Liaise with Safety Reporting and IT in all aspects of data retrieval and custom reporting.
  • Participate in inspections and audits when required.
  • Assist with related administrative and procedural activities as required or requested.
  • Independent decisions making regarding evaluating the submission of adverse event reports.
  • Ensure compliance with the training plan provided for the role.
  • Act as a buddy for colleagues and provide trainings as required

We also expect you to take an active part in the continuous development of the growing department.

 

APPLY HERE

You may be interested

Requirement of BioTech and Life Sciences Candidates at IARI
Career Biotech
14 views
Career Biotech
14 views

Requirement of BioTech and Life Sciences Candidates at IARI

Career biotech - Sep 26, 2017

Job Title : Young Professional II No.of.Posts : 1 Project Title : “Harvest Plus Biofortification of wheat”. Emoluments : Rs. 25,000/ (Consolidated) (As per ICAR F. No.17…

Requirement of Junior Research Assistant at Banaras Hindu University
Career Biotech
14 views
Career Biotech
14 views

Requirement of Junior Research Assistant at Banaras Hindu University

Career biotech - Sep 26, 2017

Job Title : Junior Research Assistant No.of.Posts : 01 Project Title : “Development of eco-friendly formulation of phyto-extracts against toxicogenic plant pathogens of Zea mays L“” Qualification…

Opening at Cipla for Senior Clinical Research Associate
Career Biotech
16 views
Career Biotech
16 views

Opening at Cipla for Senior Clinical Research Associate

Career biotech - Sep 26, 2017

Job Description Job Title : Senior Clinical Research Associate Qualification : M. Pharm or MSc in any subject or Clinical Research. MSc in Clinical Research is preferable…

Most from this category