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Senior Clinical Data Coder
Parexel International Corporation
Hyderabad, Telangana, India
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 International
Job Description Template
(TP-HR-WW-001-03)
TP-HR-WW-001-03 JD Version Date: 01-Apr-2015
Effective Date: 01 Jan 2013
Related 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 work
Education
Bachelor’s degree and / or other medical qualification or relevant Coding or Data Management experience
Language 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. Previous
relevant coding, data management work experience required; clinical and/ or research experience with solid
understanding of clinical trials methodology and terminology required.
Job posted: 2021-10-08