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| Job Location | Hyderabad |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Pharma / Biotech |
| Functional Area | Sales / BD |
| EmploymentType | Full-time |
The role of the Senior Clinical Data Coder (Sr. CDC) is to manage the performance of clinical data coding activities from database set-up through database lock on assigned projects, commensurate with experience and/or project role. Responsible for managing coding data for a moderate to large study or multiple small size studies and functioning as an SME and Principal CDC, with minimal to no supervision. In addition will provide leadership, project organization and training as SME to less experienced members of the coding team.QualificationsExcellent interpersonal, verbal and written communication skills Excellent technical skills including but not limited to the knowledge of Clinical Trial/Data Management/ Coding Systems, PMED, MS-Office products Sound awareness of all relevant regulations, including ICH-GCP, 21 CFR 11 Advanced knowledge of medical terminology and coding dictionaries (e.g.MedDRA & WHODrug)PAREXEL InternationalJob Description Template(TP-HR-WW-001-03)TP-HR-WW-001-03 JD Version Date: 01-Apr-2015Effective Date: 01 Jan 2013Related to: SOP-HR-WW-001 Page 2 of 2 Possess a thorough understanding of the various tasks related to clinical trial initiation, ongoing monitoring /processing and lock Ability to carefully weigh the priority of project tasks and to direct the team accordingly Ability to understand the strengths and development areas of team members Ability to lead a virtual global team as required Ability to reach win-win solutions to solve problems Ability to make appropriate decisions in ambiguous situations Communicate and work effectively with clients Contribute to process improvements Effective time management in order to meet team objectives Commitment and performs consistently high quality workEducation Bachelor s degree and / or other medical qualification or relevant Coding or Data Management experienceLanguage Skills Excellent in written and oral English. Excellence in regional languages as needed.Minimum Work Experience Must be able to demonstrate proficiency with all tasks from data start-up through data-base lock. Previousrelevant coding, data management work experience required; clinical and/ or research experience with solidunderstanding of clinical trials methodology and terminology required.,
Keyskills :
medical terminology21 cfrclinical datawork effectivelydata managementdata codingms officetime managementclinical trialswritten communicationtechnical skills