AddressAssociate Medical Coding Professional
Category: Data & AI
Location: Bangalore, Karnataka, IN
Department: Data Systems & Automation, Bangalore Global Development GBS (DSA,BGD)
Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If so, raise your hand as there is an exciting opportunity waiting for you as “Clinical Data Facilitator” with us. “Apply Now” At Novo Nordisk, we assure you will experience the best.
About the Department
Data Systems & Automation (DSA), Data Management, Bengaluru is one of the most competent and diverse team of professionals who are mainly responsible for providing functional and system support to execute clinical trials across Product Development Plan portfolio. The team has strong understanding of Clinical Systems & interfaces with end-to-start mindset on standardisation of data-flow across systems, Electronic Case Report Form (ECRF) development using Central Designer and knowledge with Clinical Data Interchange Standards Consortium (CDISC) concepts annotated Case Report Form (aCRF), Study Data Tabulation Model (SDTM) mapping, SAS programming, Study Data Review Guideline (SDRG) etc., to aid CDISC submission which is a mandate from regulatory authorities.
The Position
As an Associate Medical Coding Professional, 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 WHODrug 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,ensuring compliance with internal and external coding procedures by coordinating with Senior/Medical Coding Professional and Global Safety, and maintaining contact with relevant external organizations. Additionally, you will be required to report on the status of coding of clinical trials to keep all stakeholders informed. Your role will be critical in ensuring the accuracy and compliance of clinical trial data.
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- 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 Professional and Global Safety, and maintain contact with relevant external organizations
- Report on the status of coding of clinical trials
Experience
- M.Sc / B.Sc in Life Science or comparable degree in medicine, nursing, pharmacy, veterinary science or clinical information management or equivalent qualifications
- Preferably 3 years of data management experience and the majority of this within Pharma industry or Development
- Preferably knowledge of Medical Coding dictionaries
- Preferably experience in project management
- Ability and willingness to adjust quickly to new situations in a continuously developing environment
- Team oriented personality with high degree of flexibility and cross-cultural awareness
- Understanding of project management
- Knowledge of ICH/GCP and drug development preferable
Working At Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales- we're all working to move the needle on patient care.
Contact
To submit your application, please upload your CV online (click on Apply and follow the instructions).
Deadline
Apply on or before: 14th January 2024
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
