IQVIA Released Job Openings On 15/07/2022.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.Pharm,M.Pharm,B.Sc,M.Sc Graduates with 10-15+ Years Experience for Clinical Data Coder Position.Complete Details for the Clinical Data Coder as follows.
Important Details :
- Location :Bangalore/Bengaluru
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: NA
- Opening date for online Application:15/07/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
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Job Description/Skills Required
Manage single and multi-service projects, ensuring quality deliverables on time, within budget and to the customers satisfaction; Provide expert skills as part of a Clinical Data Management (CDM) team to provide quality data that meet customer needs; Provide leadership to the team in the area of coding, project planning and execution, financial management, communication and milestone tracking; Viewed as an expert in coding of clinical data; May perform the role of a Data Operations Coordinator (DOC), Data Team Lead (DTL), and a customer site lead or may be responsible for managing and delivering a program of studies for a customer.
Essential Functions
• Serve as an account lead, or internal or external point of contact on standalone coding studies or accounts
• Manage the customer relationship for the project team including active participation in coding related customer negotiation on timeline, budgetary and other issues
• Provide leadership and senior support to lead coders on one or more large global studies
• Manage the relationship with a customer on a DM site level
• Serve independently as a Lead Data Coder and/or Coding reviewer for one or more projects
• May serve as a DOC or DTL for one or more projects
• Perform comprehensive quality control procedures
• Perform Serious Adverse Event (SAE) reconciliation activities
• Collaborate with customers and develop solutions and action plans for issues, escalations and
Qualifications
• Pharmacy, dental, medical, nursing, life sciences or related field qualification or educational equivalent
• 7 years relevant experience in clinical trials within a similar function, including proven competence in managing the delivery of coding or/and other data management processes for multiple global projects, also including experience in handling complex customer negotiations and bid defense meeting..
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