Novo Nordisk Recruitment Clinical Data Manager in Global Development team

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Novo Nordisk Recruitment June 2020 M. Sc / B. Sc degree in Life Science or comparable degree in medicine, nursing, pharmacy, veterinary science or clinical information management or equivalent qualifications. for Clinical Data Manager in Global Development team @ India Bangalore, Karnataka, IN. Interested candidates Apply online for selection as Full detailed below.

Vacancy details:

  • Post Name: Clinical Data Manager in Global Development team
  • Qualification: M. Sc / B. Sc degree in Life Science or comparable degree in medicine, nursing, pharmacy, veterinary science or clinical information management or equivalent qualifications.
  • Experienced:You are expected to have deep 2-3 years of data management experience and the majority of this within Pharmaceutical Industry or Development and 2 years of experience in information technology and good knowledge of Clinical Development.
  • Location: India Bangalore, Karnataka, IN
  • Salary :NA
  • Openings :NA

 Job Description: We have requirement for the post of Clinical Data Manager in Global Development team in Novo Nordisk !Contact:For further information, please contact Shivalingappa at SVGK@novonordisk.com

The Position:
As Clinical Data Manager your key responsibility is to coordinate and support the main Data Management roles for the trial in ensuring DM documentations, Data handling including timely completion of discrepancy management activities for assigned projects following appropriate regulatory guidelines, company and department SOPs

Simultaneously, the role will also include Ensuring the integrity of clinical trial databases, perform data validation for ensuring completeness and make data availability to relevant stakeholders by generating reports in a timely manner and also ensure good documentation practices are followed.

Handle interim analysis as directed by the trail data manager depending on the trial characteristic. Also as Clinical Data Manager you need to be in alignment with Trial Stakeholders to identify risks and incorporate preventive/mitigating plan. And also you should secure that all trial work is adhered to current DM standards. This includes in the trial set up phase: Laboratory set up (incl. lab parameters), paper CRF and eCRF modules, global validation/derivation procedures in CDMS/EDC and standard annotations.

Selection ProcessThe selection will be on the basis of Interview.

How to Apply :     Click here for full details and apply online




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