Freshers Life Sciences Job at Novo Nordisk – Apply Online
Freshers Life Sciences Job at Novo Nordisk – Apply Online. MSc Life Science candidates are eligible to apply online for an Associate Non-clinical Report Analyst in Global Development position that is available at Novo Nordisk, which is one of the world’s most successful pharmaceutical companies and with great growth potential.
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Novo Nordisk Vacancy Details
Designation: Freshers Life Sciences Novo Nordisk Report Analyst Recruitment
Category: Clinical Development and Medical
Location: Bangalore, Karnataka, IN
As Associate Non-clinical Report Analyst you are responsible to perform eCTD checks of reports including but not limited to Non-clinical CRO Reports, Non‑clinical Section Reports for Clinical Trial Reports, Non-clinical Principal Investigators Reports, Clinical CRO Reports for Clinical Trial Reports etc. Receive the report through the TripleS assignment web or from the Sponsors Monitor through the TripleS assignment web on Globeshare based upon the report type and also perform the eCTD check of the PDF version of the report according to internal PDF check list based upon the report type – map and also describe all issues identified in the report and communicate this to the SponsorsMonitor or correct the issues identified in the document and communicate to the Principal Investigator if necessary to ensure compliance with Novo Nordisk standards for eCTD compliant reports.
For CRO reports, perform a second review of the report to follow up on their quality as well as communicate to sponsors keep track of if the report is acceptable and perform indexing of the final signed report or start the signature workflow in novoDOCS as appropriate by ensuring all workflows, procedures, checks and standards are followed based on the report type and in compliance with NN QMS, which can make sure quality and also timeliness of the eCTD checks with focus on stakeholder and also organisational requirements for Non-clinical Reports based on the current Novo Nordisk standards for eCTD compliance.
You are expected to have the below abilities as well as knowledge:
- Master’s in Life Science, Computers/IT, Engineering etc. or equal degree or professional experience
- 0-2 years of industry experience
- Experience in the use of Document Management Equipment, Adobe Acrobat Professional and also MS tools: Outlook, Excel, Word, and PowerPoint
- Excellent knowledge of clinical development, good knowledge in GLP, eCTD and ICH standards is desirable
- Team player with a high degree of flexibility
- Ability to multitask and also prioritize activities
- Live up to Novo Nordisk Way
- Excellent communication abilities
Contact: For further information, please contact Shiva K at [email protected]
Deadline: 05 Sep 2020
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