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Posted 1 weeks agoCoding Specialist II
at Fortrea
Bangalore, IndiaOn-site
Responsibilities
- Develop and maintain a close liaison with project Lead Data Reviewer, core team members, and Clinical Lead Data Managers as appropriate. Summary of
- Interact and collaborate with other project and specialty team members (clinical, programming, statistics, Clinical Data Management, drug safety, etc.) to support the set-up, maintenance, and closure of the data management aspects of the project to ensure consistent, cohesive data handling and quality of coded clinical data.
- Maintain coding technical competencies via participation in internal and external training seminars.
- Support project staff on achieving client satisfaction (internal and external) through delivery of quality medical coded data, on-time, and on-budget.
- Perform dictionary verification on assigned projects.
- Review literature and research technologies/procedures for improving global thesaurus management practices.
- Perform the clinical medical data coding aspects of assigned projects on a global basis independently.
Requirements
- Assist with the dictionary verification of Fortrea standard dictionaries and client dictionaries in a timely manner.
- Qualifications (Minimum Required): University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., professional registered nursing certification, medical or laboratory technology).
- Fortrea may consider relevant and equivalent
- experience in lieu of educational requirements. Fluent in English, both written and verbal.
- Experience (Minimum Required): Minimum (5-7) years relevant work experience in clinical data coding experience (MedDRA and WHODrug).
- In-depth knowledge of medical coding process and various coding tools (e.g., Medidata Coder, Central Coding, etc.).
- In-depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.
- Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.
- Broad knowledge of thesaurus management process.