IQVIA Clinical Data Management Jobs

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IQVIA Clinical Data Management Jobs
- IQVIA invites applications for the post of Assoc Clinical Data Manager. Interested & eligible candidates need to apply online via the official website.
About IQVIA: we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions, and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way.
IQVIA Clinical Data Management Jobs
Organization Name  IQVIA
Post Name Assoc Clinical Data Manager
Job ID R1159889
Job Type Full Time
How To Apply Online
Official Website iqvia.com
IQVIA Clinical Data Management Vacancy Details
Clinical Data Management Job Description:
  • Interprets the study protocol.
  • Design and update the eCRF.
  • Create and update Edit Specification Document.
  • Generate specifications for EDC build components (e.g., Rights and Roles, System Settings and Home Page)
  • Complete the Study Authorization Form and Trial Capacity Request Form (InForm)
  • Attend the Pre-Design Meeting, Online Screen Review Meeting, Unblinded Data review meeting. Attend and present comments at the Internal Design Review Meeting. May lead Online Screen Review Meeting.
  • Facilitate the internal Edit Specification Review Meeting and leads the discussions regarding the Edit Specification Document.
  • Design the database to collect LLRR data within the InForm database and ensure Rights and Roles document has appropriate access for Entry and Updates.
  • Communicate any project risks to the Data Team Lead, including the potential for missing a timeline in the Data Management Project Plan.
  • Escalate potential quality issues.
  • Ensure the completion and documentation of all project-specific training, as well as staying current with required Standard Operating Procedures.
  • Reviews build timelines and provide input as applicable.
  • Reviews QIP for own projects, identify out of scope activities if any and inform relevant parties.
  • Responsible for multiple study design projects at the same time.
  • Might be working on projects across multiple platforms.
  • Identify areas for process improvements on an ongoing basis. Actively take part and contribute towards process improvement initiatives as assigned besides providing suggestions for continuous improvement of processes.
CDM Job Requirement:
  • Good understanding of the clinical research process
  • Excellent Communication
  • Edit check, eCRF designing, listings, writing will be preferred.
  • Worked on startup, post-production changes or migration
  • Any platform (Rave/Inform/Oracle/YDOC or any other platforms)
Selection Process:
  • Based on Written / Personal Interview as per company norms.
Pay Scale:
  • NA
Job Location:
  • Kochi, India (INKOC2, 42.5),IND;Thane, India (INMUM1, 42.5),IND
Editor’s Note: IQVIA Clinical Data Management Jobs. Please make sure that you are subscribed to the TyroPharma Newsletter (*to Activate Subscription Verify Link in your E-Mail inbox*) to be notified of all of the latest & Upcoming Vacancies. Follow us on social media Facebook, Twitter, LinkedIn, WhatsApp, Telegram

FAQ's
What is clinical data management job?
Clinical Data Management is the collection, integration, and validation of clinical trial data.
Clinical data management jobs salary?
The Average salary range between 2.9L - 10L per year.
Why is clinical data management important?
To review, and approve the latest drugs by Regulatory Agencies depends upon a trust that clinical trial data presented are of sufficient integrity to make sure confidence in results & conclusions presented by the pharma company.
Members involved in Clinical Data Management?
Following are the key members involved in Data Management:
  • Project Manager / Data Manager
  • Database Administrator
  • Database Programmer / Developer
  • Clinical Data Associate

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