Work as Senior Clinical Coding Specialist at Novartis | B.Pharm

Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.

Post : Senior Clinical Coding Specialist

Job Description
Provide timely and professional ongoing management of clinical trial data by performing accurate and consistent coding, providing inputs to the relevant coding sections of the Data Management Documents and reviewing coding glossaries. Provide Functional/technical Coding leadership for multiple trials or mega trials in the role of Program Coder. Leads/Coordinates synonym review activities and dictionary version upgrade activities at trial/Program level.

Key Responsibilities:
• Performs accurate/consistent coding, applying standard conventions, creating appropriate synonyms, creating/closing coding-related queries, and interacting with TDMs/CTHs/Medics/others as needed
• Specific responsibility of Leading/managing synonym review/update processes and Dictionary version upgrades at trials/project level.
• Ensures that coding is completed in support of all timelines/deliverables and Coding related section(s) of data management documents are up to date.
• Troubleshoots coding problems, collaborating with peers, database developers, and/or IT support as needed
• Effectively represents the Coding in the CTT meetings or in communications with the stakeholders.
• Coach, mentor and develop the new joiners technically, may serve as an SME for Coding

Candidate Profile
• University or college degree in life science, chemistry, pharmacy, nursing, or equivalent relevant degree. Advanced Pharmacy degree preferred with 4 or more years of experience in drug development with at least 3 years performing Clinical coding.
• Demonstrated ability to adapt to different coding technologies
• Expert level of knowledge of medical terminology, including medical conditions and medications. Strong attention to detail.
• Strong verbal and written communication skills, including ability to author Coding conventions, SOPs/WPs, and training materials
• Good problem-solving, negotiation and conflict resolution skills. Ability to work independently, under pressure, and in an environment where flexibility is required.
• Understanding of clinical trials methodology, GCP, system validation requirements, and coding tools.

Additional Information
Experience : 4+ years
Qualification : University or college degree in life science, pharmacy, chemistry
Location : Hyderabad, AP
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Research & Development
End Date : 25th May, 2021