Icon Clinical Research Virtual Career Drive On 8th,9th,15th & 16th Sept 2022

Icon Clinical Research Released Job Openings On 27/08/2022.Icon Clinical Research Limited is an Indian multinational corporation that provides information technology, consulting and business process services. The Fortune India 500 ranks it the 29th largest Indian company by total revenue. It is also ranked the 9th largest employer in India with over 221,000 employees.Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Icon Clinical Research Recruitment 2021 are provided below. Interested and eliible candidates can  submit application along with resume. 

Vacancy Details:

Icon Clinical Research Hiring Any Graduate with 02 –07 Years of Experience for Clinical Data Coordinator II/Sr.Clinical Data Coordinator Position.Complete Details for the Clinical Data Coordinator II/Sr.Clinical Data Coordinator as follows..

Important Details :

• Location : Chennai, Bangalore & Trivandrum
• No of Vacancies:NA
• Details of Salary: NA
• Opening date for online Application:27/08/2022
• Mode of application :Online
  
• How To Apply: CDC II – 8th & 9th September,CDC II & Senior CDC -15th & 16th September,reach out to me directly Rajkapoor Kamaludeen or Register yourself for our #Virtual Career Event: https://lnkd.in/gHHJzT3S

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Job Description/Skills Required

• Recognize, exemplify and adhere to ICON’s values which center around our commitment to People, Clients and Performance.
  • As a member of staff, the employee is expected to recognize the importance of and create culture of process improvement with a focus on streamlining our processes adding value to our busin ss and meeting client needs.
  • Travel (approximately 0%) domestic and I or international.
  • Read, ensure understanding and adhere to all assigned ICON SOPs and working pr cedures.
  • Ensure all work performed is of high quality, compliant with Good Clinical Practice, ICH Guidelines and all applicable laws and regulations.
  • Complete all assigned trainings (including the Study Lead Development program) and co rses in the ICON Training Management system (iLearn); ensuring that mandatory courses are all completed before the designated date and that the required system specific training has been co pleted for current studies.
  • Record all billable and non-billable time in the appropriate timesheet management s stem (e.g. Planview).
  • Review CRF I eCRF data for completeness, accuracy, and consistency via computerize edits and manual data checks.
  • Perform external data reconciliation .
  • Perform Serious Adverse Event reconciliation .
  • Generate and close/resolve (as appropriate) data queries .
  • Freeze and/or lock eCRFs (as appropriate) within the Electronic Data Capture System.
  • Create and maintain study files and other appropriate study documentation .
  • Perform User Acceptance Testing and collaboratively work with CDMS personnel to see i ues found through re-testing and resolution.
  • Assist Data Management Study Lead in development of eCRF, Data Validation Specific tions, and Study Specific Procedures.
  • Train and guide less experienced CDCs in data management requirements and activities.
  • Perform other project activities as required in order to ensure that study timelines a e met (for example, filing and archiving of study documentation , dispatching of queries to investigate or sites for resolution, etc.).
  • As required, communicate effectively with the Project team, Study Lead, Project Lead nd Project Manager.

Click here for Official notification and Apply