IQVIA Released Job Openings On 26/03/2022.The Company offers commercial, physical, and biological research and development services, as well as value-based analyses, research studies, clinical management analytics, and health outcome optimization services.Application form link provided at the end of post. Eligibility for the Clinical Data Coder as follows.
Vacancy Details:
IQVIA Recruiting B.Pharma/M.pharma/B.sc/M.sc Candidates with 02+ years of Experience for Clinical Data Coder Position.Complete Details for the Clinical Data Coder as follows.
Important Details :
- Location : Thane, Bangalore/Bengaluru
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application: 26/03/2022
- Mode of application :Online
- How To Apply: Share your updated CV to babymoni.changmai@iqvia.com
Related Job: Alembic Pharmaceuticals Walk In Interviews On 30th March 2022Â
Job Description/Skills Required
Job Description Summary
Provide comprehensive data management expertise (defined as efficient and quality data management products) to Data Management (DM) team to meet sponsor and company needs. Perform Clinical Data Management and/or Coding activities, and may provide leadership either in the role of the Lead Coder or in a specific CDM task (e.g. Data Operations Coordinator (DOC) or lead a coding related task on a mega trial).
Essential Functions• Serve independently as a Clinical Data Coder and/or Lead Coder or DOC for one or more protocols.
• Manage delivery of coding activities and/or stand alone coding projects through full study life-cycle (with minimal guidance).
• Validates/tests the coding application and programming of coding reports
• may also test coding related datasets, coding related edits or any coding related programming activities.
• Perform comprehensive data management and coding related tasks including, conducting data review and writing and resolving data clarifications.
• Manage coding related project timelines with guidance from the DOC or Data Team Lead (DTL) or Manager.
• Perform Serious Adverse Event (SAE) reconciliation activities.
• May serve as a back-up for a Lead Coder, DOC or DTL.
• Perform comprehensive quality control procedures, Assist in implementing new technology.
• Independently bring coding and project related solutions to the DM team.
• Handle audit requirements for respective studies including stand-alone coding projects as applicable.
• Understand and comply with core operating procedures and work instructions.
• Perform other duties as directed by the study team or Manager, or meet objectives as assigned
• Develop and maintain good communication and working relationship with the team.
Click here for Official notification and ApplyÂ
