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Sr. Medical Coder

3.00 to 6.00 Years   Chennai   04 May, 2021
Job LocationChennai
EducationNot Mentioned
SalaryNot Disclosed
IndustryFMCG / F&B
Functional AreaOperations Management / Process Analysis
EmploymentTypeFull-time

Job Description

The role of Senior medical coder is to perform assigned tasks or activities in clinical data coding. Activities may include UST, coding, data validation, generation and integration of queries, running of reports.Primary ResponsibilitiesEnsure that coding services offered by the company are carried out with consistent quality by :

  • Demonstrating full competence when performing the following tasks:
  • Clinical data coding
  • Generate and integrate data coding queries
  • Conduct clinical coding review of coding performed by internal Data Management staff
  • Create coding conventions
  • Work with data management team and data management customers to assure that coding is performed per clinical coding guidelines, customer specific guidelines and internal SOPs
  • Test data creation and UAT
  • Validation and cleaning of the coded data
  • Conduct data reconciliation
  • Carry out all the coding related tasks throughout the Data Management lifecycle of the project with minimal assistance
  • Being responsible for timely and quality delivery of clinical data.
  • Acting as single point of contact (internal expert) for specific processing task(s) on a project.
  • Other assigned responsibilities per business requirement.
Maintains quality service and departmental standards by:
  • Adhering to CDM processes and standards by using implemented systems
  • Reading, understanding and adhering to organizational Standard Operating Procedures (SOPs)
  • Participating in the modification of company SOPs related to CDM Services
Secondary ResponsibilitiesContributes to team effort by:
  • Working with internal staff to resolve issues
  • Exploring new opportunities to add value to organization and departmental processes
  • Helping others to achieve results
  • Performing other duties as assigned
Maintains Technical and Industry Knowledge by:
  • Attending and participating in applicable company-sponsored training
QualificationsEducation:
  • Associate s degree required, Bachelor s preferred, in the life sciences or a related field
Experience:
  • 3.5 years of medical coding experience or working with clinical trials and/or within pharmaceutical environment
  • Understanding of medical and/or clinical trial terminology required
  • Proven ability in analyzing data
  • Experience working with computer software including Word, Excel and Access preferred
Additional skill set:
  • Ability to work in group setting and independently; ability to adjust to changing priorities
  • Excellent attention to detail and orientation toward meticulous work
  • Strong interpersonal and communication skills, both verbal and written
  • Strong documentation and organizational skills
  • Ability to project and maintain a professional and positive attitude
  • Knowledge of medical terminology and awareness of coding dictionaries (e.g. MedDRA & WHODRUG)
  • Ability to plan tasks and complete them, within appropriate time scale and to the required quality
  • Effective time management in order to meet the team objectives.
Working ConditionsTravel: 0-10%Lifting: 0-15lbsOther: Computer work for long periods of timeEEO StatementBioclinica is an equal opportunity employer. Bioclinica evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.Collaboration, Continuous Learning, Critical Thinking, Organizational Awareness, Results Orientation, Service Orientation,

Keyskills :
cpticdmedical codingprogrammingstandard operating proceduresdata codingmusic makinglife sciencesclinical datadata managementclinical trialsdata validationtime managementcritical thinkingicd10

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