Opening for Life science Freshers as Associate Standards Supporter @ Novo Nordisk
Are you a person with innovative thinking and proactive attitude with continuous improvement as one of your career objectives?Join Global Development (GD) Team at Novo Nordisk and get a life-changing career ! About the department : GD -GSC-Clinical DM Support Unit supports Projects and Trial Management on DM tasks that are other than operational data management activities on clinical projects. These includes functions and roles covering Functional Supporters, eLoader, ePRO Operations Specialist, mynovotrial.com Administrator, Titration report specialist, EDC Report Specialist, EDC-IVRS Interface Specialist, EDC Ops Specialist, Change Manager, CDW – Standards Supporter, CMC Coordinator, Trial Data Coordinator etc. All in all it’s a Dynamic, Diverse and Vibrant unit committed to ClinOps mission of “We unite People, Performance, and Process together” team with a fall-back infrastructure of good clinical and technical knowledge.
Job Title: Associate Standards Supporter
Job Description:
Mapping of clinical data and metadata from source system(s) to CDW
Review of (e)CRFs and DCM annotation. Special attention should be given to non-standard modules regarding impact on OC and CDW setup
Map data from IMPACT and OC to CDW ensuring consistency and correctness according to the CDW data model. The Global Library in CDW should be used as basis
Request codes/topic codes as needed
Request changes to OC study setup as needed
Ensure that all data on a trial level is mapped and review the mappings by using the relevant UAT reports
Document the annotation from IMPACT/OC to CDW
Maintain and improve database architecture
Setup global mappings as assigned within the mapping team
Maintain documentation for global mappings
Update documentation related to the system as appropriate
Maintain documentation for codes (controlled terminology)
Qualifications: M.Sc / B.Sc in Life Science or comparable degree in computer science, Information Technology clinical information management or equivalent qualifications.
Experience: 0-2 years in pharmaceutical industry and preferably 1 year within clinical data management systems. Expert general knowledge of computer systems and IT. Knowledge of drug development and basic medical terminology. Knowledge of GxP and guidelines within drug development.
Click here to apply
Are you a person with innovative thinking and proactive attitude with continuous improvement as one of your career objectives?Join Global Development (GD) Team at Novo Nordisk and get a life-changing career ! About the department : GD -GSC-Clinical DM Support Unit supports Projects and Trial Management on DM tasks that are other than operational data management activities on clinical projects. These includes functions and roles covering Functional Supporters, eLoader, ePRO Operations Specialist, mynovotrial.com Administrator, Titration report specialist, EDC Report Specialist, EDC-IVRS Interface Specialist, EDC Ops Specialist, Change Manager, CDW – Standards Supporter, CMC Coordinator, Trial Data Coordinator etc. All in all it’s a Dynamic, Diverse and Vibrant unit committed to ClinOps mission of “We unite People, Performance, and Process together” team with a fall-back infrastructure of good clinical and technical knowledge.
Job Title: Associate Standards Supporter
Job Description:
Mapping of clinical data and metadata from source system(s) to CDW
Review of (e)CRFs and DCM annotation. Special attention should be given to non-standard modules regarding impact on OC and CDW setup
Map data from IMPACT and OC to CDW ensuring consistency and correctness according to the CDW data model. The Global Library in CDW should be used as basis
Request codes/topic codes as needed
Request changes to OC study setup as needed
Ensure that all data on a trial level is mapped and review the mappings by using the relevant UAT reports
Document the annotation from IMPACT/OC to CDW
Maintain and improve database architecture
Setup global mappings as assigned within the mapping team
Maintain documentation for global mappings
Update documentation related to the system as appropriate
Maintain documentation for codes (controlled terminology)
Qualifications: M.Sc / B.Sc in Life Science or comparable degree in computer science, Information Technology clinical information management or equivalent qualifications.
Experience: 0-2 years in pharmaceutical industry and preferably 1 year within clinical data management systems. Expert general knowledge of computer systems and IT. Knowledge of drug development and basic medical terminology. Knowledge of GxP and guidelines within drug development.
Click here to apply
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