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Job Location | Hyderabad |
Education | Not Mentioned |
Salary | Not Disclosed |
Industry | Medical / Healthcare |
Functional Area | SBU Head / CEO / DirectorBio Tech / R&D / Scientist |
EmploymentType | Full-time |
Job Description Your responsibilities: Your responsibilities include, but are not limited to: 1. Selects, recruits, develops, manages, motivates, coaches and appraises the performance of direct reports, to ensure high quality performance across his/ her Clinical Data Management group. 2. Builds and establishes a strong team spirit and creates a team founded on technical ability, excellence in performance and trust 3. Facilitates a partner and customer orientated Clinical Coding Group, role modelling behaviors for more junior members of staff 4. Serves as the owner of the Coding Systems and Dictionaries, liaise with the IT, system provider and Dictionary provider. 5. Manages and co- ordinates the assignment of resources across the portfolio. Ensures that coding is completed in support of all timelines/ deliverables 6. Provides all necessary support to help address and resolve issues 7. Manages dictionary upgrades within the system and trials in line with company priorities and Health Authorities/ Novartis guidelines 8. Manages dictionary upgrades within the system and trials in line with company priorities and Health Authorities/ Novartis guidelines 9. Understands Health Authority requirements from Coding & Dictionaries perspective and is able to participate in Health Authority inspections as required 10. Effectively represents the Coding Team in process improvement initiatives, system update efforts, strategic initiatives and operating policies. 11. Serves as a Coding SME Minimum requirements University or college degree in life science, computer science, pharmacy, nursing or equivalent relevant degree. English 10 or more years of experience in drug development with at least 8 years performing Clinical coding. Ability to effectively lead teams 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 Understanding of clinical trials methodology, GCP, system validation requirements, and coding tools. ,
Keyskills :
customerterminologynegotiationmedicalclinicalcodingdevelopmenttrategicplanningstrategicdirectdrug