Novo Nordisk Senior Clinical Data Manager in Global Development
team M. Sc / B. Sc degree in Life Science or comparable degree in medicine,
nursing, pharmacy, veterinary science
The Position:
As Senior Clinical Data Manager your key responsibility is to
strategize execution of clinical trial and clinical trial business processes
which includes execution of clinical projects and handle Quality Control (QC)
documents.
Simultaneously, the role will also include to involve
yourself in the process of outsourcing and collaboration with vendors/Clinical
Research Organization (CRO). In addition, you will be responsible for managing
projects related to clinical trials and follow data management standards of
validation and derivation procedures.
Additionally, you will be involved in large complex trials
and strategize the team with knowledge about drug development process.
Key success criteria will be to become an expertise in data
programming languages and tools which includes to understand the interface and
integration between OC - TMS – EDC system – IVRS. You hold and 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 the Novo Nordisk Way.
Hence, a strong understanding of data management and clinical
trial, being able to generate new ideas, providing thorough analysis, formulate
and present recommendations will be expected to drive GCP expectations.
Qualifications
As a person you are ambitious, proactive and ability to
interact with people at all levels in the organisation. You hold a M. Sc / B.
Sc degree in Life Science or comparable degree in medicine, nursing, pharmacy,
veterinary science or clinical information management or equivalent
qualifications.
You are expected to have deep strategic knowledge of clinical
development, medical coding and CRF design, preferably 4-5 years of data
management experience and the majority of this within Pharma Industry
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