Novo Nordisk is hiring B. Pharma/ M. Pharma/ B. Sc/ M. Sc/ BV Sc as Associate Medical Coding Professional – Apply Now

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Are you a skilled professional in pharmacy, nursing, life sciences, or veterinary sciences? Novo Nordisk is actively seeking talent like yours for the role of Associate Medical Coding Professional in Bangalore. Join our dynamic team and contribute your expertise to the exciting field of medical coding. Explore this rewarding opportunity with Novo Nordisk today!
Job Title Associate Medical Coding Professional
Category Data & AI
Department Data Systems & Automation (DSA)
Qualifications M.Sc / B.Sc in Life Science or comparable degree in medicine, nursing, pharmacy, veterinary science, or clinical information management or equivalent qualifications
Experience Preferably 3 years of data management experience, with the majority of this within the Pharma industry or Development.
Preferably knowledge of Medical Coding dictionaries.
Preferably experience in project management.

 

Skills

  • Ability and willingness to adjust quickly to new situations in a continuously developing environment.
  • Team-oriented personality with a high degree of flexibility and cross-cultural awareness.
  • Understanding of project management.
  • Knowledge of ICH/GCP and drug development preferable.

The Position

As an Associate Medical Coding Professional, your primary responsibility will be to perform timely and accurate categorization of verbatim text in assigned clinical trials to standard medical dictionaries and nomenclature such as MedDRA and WHO Drug Global using the TMS Application. You will also be responsible for performing ATC coding on concomitant medications with multiple ATC codes based on project/trial requirements. Additionally, you will ensure compliance with internal and external coding procedures by coordinating with Senior/Medical Coding Professional and Global Safety, and maintain contact with relevant external organizations. Reporting on the status of coding of clinical trials will also be part of your role.

Key responsibilities:

  • Perform timely and accurate categorization of verbatim text in assigned clinical trials to standard medical dictionaries and nomenclature (MedDRA and WHODrug Global) using the TMS Application.
  • Perform ATC coding on concomitant medications with multiple ATC codes based on project/trial requirements.
  • Ensure compliance with internal and external coding procedures by coordinating with Senior/Medical Coding Professionals and Global Safety, and maintain contact with relevant external organizations.
  • Report on the status of coding of clinical trials.

About the department

Data Systems & Automation (DSA), Data Management, Bengaluru, is a highly competent and diverse team of professionals responsible for providing functional and system support to execute clinical trials across the Product Development Plan portfolio. The team possesses a strong understanding of Clinical Systems and interfaces, with an end-to-start mindset focused on standardizing data flow across systems. They excel in Electronic Case Report Form (eCRF) development using Central Designer and possess knowledge of Clinical Data Interchange Standards Consortium (CDISC) concepts, including annotated Case Report Form (aCRF), Study Data Tabulation Model (SDTM) mapping, SAS programming, Study Data Review Guideline (SDRG), among others. These skills are crucial for aiding CDISC submission, which is a mandate from regulatory authorities.

Location Bangalore, Karnataka, IN
Apply Now Click Here
Last Date 30th May 2024

 

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