location_onBengaluru, Karnataka, India
watch_later Posted: Jul 18, 2024
Skills Required
Nice To Have skills
Job Description
About the job
Job description:
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us.
A great opportunity has opened within the Data Monitoring, Management and Innovation department to further strengthen our Medical Coding team.
Your role:
• Perform medical coding of clinical data such as adverse events, concomitant medications, and medical history using MedDRA and WHODrug global dictionaries as per agreed coding guidelines. This includes reviewing of automatically coded data by a coding tool as well as performing manual coding of data that cannot be auto coded by a coding tool.
• Perform review of medical coding completed by CRO or another medical coder.
• Perform medical coding and up-versioning for legacy data and pooled data. Ensure coding accuracy and consistency within studies.
• Liaise with internal Data Management team as well as CRO Data Management team to resolve any coding related data issues
Further, you:
• Contribute to the continuous improvement of processes, tools, technologies, standards, Standard Operating Procedures (SOPs) and other Quality Documents
Who you are:
• Industry Experience in the area of medical coding (minimum 7-9 years)
• In-depth experience with coding dictionaries such as MedDRA, WHODrug
• In-depth experience with coding tools and processes
• Fluency in English (oral and written)
• Detail orientation with strong prioritization skills
• Sound understanding of the activities of trial and development team
• Comprehensive knowledge of ICH-GCP, FDA regulations and Good Clinical Practice
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