Novo Nordisk Life Science

Novo Nordisk Life Science Clinical Data Manager Job Recruitment

Novo Nordisk Life Science Clinical Data Manager Job Recruitment. Life Sciences candidates are eligible to apply online for a Senior Clinical Data Manager in Global Development team 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: Senior Clinical Data Manager in Global Development team

Category: Clinical Development and Medical

Location: Bangalore, Karnataka, IN

Are you searching for the opportunity to make our patients’ lives better and also leave your footprint! Then perhaps you are the “Senior Clinical Data Manager” we require for an exciting project.

Regarding the department:

The data management department was established in Bangalore, India in the month of September 2007 as well as has actually considerably grown from 10 members to a strong team of over 119 Clinical Data Management professionals. It has witnessed significant transformations right from providing DM services to IO region reporting to IOCDC to becoming an integral part of Global development from Aug 2010. It is a young, enthusiastic and dynamic team with different skillsets and 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 high quality data delivery to the stakeholders. The involvement of numerous groups in data management is significant in key stages of trial setup, conduct and closeout.

The Position:

As Senior Clinical Data Manager your key responsibility is to strategize execution of clinical trial as well as clinical trial business processes that includes execution of clinical projects and handle Quality Control (QC) documents.

Simultaneously, the role will certainly additionally consist of to involve yourself in the process of outsourcing and collaboration with vendors/Clinical Research study Organization (CRO). On top of that, you will be accountable for managing projects associated with clinical trials and also follow data management standards of validation and also derivation procedures.

Additionally, you will be involved in big complicated trials as well as strategize the team with knowledge about drug development process.

Key success criteria will be to become an expertise in data programming languages as well as tools that includes to understand the interface and also integration in between OC – TMS– EDC system– IVRS. You hold as well as strive to have a good collaboration with stakeholders and take responsibility to perform tasks independently and in accordance with Novo Nordisk SOPs, Novo Nordisk policies and also the Novo Nordisk Way.

For this reason, a strong understanding of data management as well as clinical trial, being able to produce new ideas, providing complete evaluation, develop and existing recommendations will certainly be anticipated to drive GCP expectations.

Qualifications:

  • As an individual you are ambitious, proactive as well as ability to interact with people at all levels in the organisation. You hold an M.Sc/ B.Sc degree in Life Science or comparable degree in medicine, nursing, pharmacy, veterinary science or clinical info management or comparable qualifications.
  • You are anticipated to have deep strategic knowledge of clinical development, medical coding and CRF design, ideally 4-5 years of data management experience as well as most of this within Pharma Industry.

Get in touch with

For more info, please get in touch with Sunidhi at [email protected].

Deadline: 13-May-2020

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