PRAHS

CDC II

Posting Locations IN-Bangalore
Posted Date 19 hours ago(8/5/2025 8:33 AM)
ID
2025-119514

Overview

As a Senior CDC / CDC II you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Senior CDC / CDC II is the point of contact for day to day activities on a study with key responsibilities to handle the study independently. Reporting to Group Lead/Manager.

Responsibilities

What you will be doing:

Recognize, exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance
As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs
Read, ensure understanding and adhere to all assigned ICON SOPs and working procedures
Ensure all work performed is of high quality, compliant with Good Clinical Practice, ICH Guidelines and ll applicable laws and regulations
Complete all assigned training (including the Study Lead Development Program) and courses in the ICON Training Management system (i earn); ensuring that mandatory courses are all completed before the designated date and that the required system specific training has been completed for current studies
Record all billable and non-billable time in the appropriate timesheet management system (e.g. Planview™)
Review CRF/eCRF data for completeness, accuracy, and consistency via computerized 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 issues found through re-testing and resolution
Perform other project activities as required in order to ensure that study timelines are met (for example, filing and archiving of study documentation, dispatching of queries to investigator sites for resolution, etc.)
As required, communicate effectively with the project team, Study Lead, Project Lead and Project Manager

Qualifications

  • University or college degree in life science, computer science, pharmacy, nursing or equivalent relevant degree.
  • 4 Years+ experience in Core DM activities [must have]. 
  • Ability to work under pressure demonstrating agility through effective and innovative team leadership
  • Excellent interpersonal skills and proven ability to operate effectively in a global environment. Ability to influence and communicate across functions and to external stakeholders
  • Excellent problem-solving skills
  • Excellent verbal and written skills


What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others



Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Options

Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
Share on your newsfeed

Connect With Us!

Not ready to apply? We get it! Click here to stay in touch for future opportunities, events and other happenings!