Freshers Life Science Job at Novo Nordisk – Clinical Documentation Associate Post

Freshers Life Science Job at Novo Nordisk – Clinical Documentation Associate Post

Freshers Life Science Job at Novo Nordisk – Clinical Documentation Associate Post. Life Sciences candidates are eligible to apply online for a Clinical Documentation Associate 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: Clinical Documentation Associate in Global Development

Category: Clinical Development and Medical

Location: Bangalore, Karnataka, IN

The position at Novo Nordisk:

We are looking for a Clinical Documentation Associate in the Global Development (GD) unit based out of Global Service Centre (GSC), Bangalore, India. You can anticipate an exciting job driving different projects and engaging with multiple stakeholders at the global level.

Concerning the department for the Novo Nordisk Vacancy:

The data management department was established in Bangalore, India in the month of September 2007 as well as has actually dramatically grown from 10 members to a strong team of over 119 Clinical Data Management professionals. It is a young, enthusiastic and dynamic team with varied skillsets as well as professionals from diverse backgrounds such

as Pharmacy, Life-Sciences, Physiotherapy, Computer/Information Sciences and also Business Administration. The key objective of the department is to make certain top quality data delivery to the stakeholders. The involvement of various groups in data management is significant in key stages of trial setup, conduct and closeout.

About the Novo Nordisk Vacancy:

The main job task in this role is to perform data entry of Clinical trial data from paper case report forms to the clinical database according to project timelines with an acceptable level of quality. In this position, you will certainly make sure efficient handling of Case Report Forms (CRFs) according to Novo Nordisk Standard Operation Procedures (SOPs) and departmental requirements from receipt until archival. You will certainly likewise perform Scanning, Scaling and also preparing trial level CRFs by segregating into Clinical Trail Report (CTR) as well as non-CTR subjects as well as support Electronic Case Report Forms (eCRFs) preparation for submission deliverables at the project level to make them Electronic Common Technical Document (eCTD) compliant and also on Clinical Data Interchange Standards Consortium (CDISC) document preparations.

The tasks of the Clinical Documentation Associate will, to a huge extent, be performed independently and also according to Novo Nordisk SOPs, Novo Nordisk policies as well as the Novo Nordisk Way. The Clinical Documentation Associate is recognised as in charge of supporting end users and have to act independently, following the strategic objectives of the standards governance bodies and also the company as a whole as well as has no budgetary duties.

Qualification for Novo Nordisk Vacancy:

You are expected to have the below skills as well as knowledge.

• Bachelor’s degree preferably in Life Science or comparable degree in Computer Science, Information Technology, Clinical Info Management or comparable qualification
• 0-1 year data entry experience; ideally on clinical database systems
• Computer literacy as well as proficient in Microsoft Office tools

Get in touch with

For further info, please get in touch with Shivalingappa– [email protected]

Deadline: 30 April 2020

APPLY ONLINE

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