CDC II
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a CDC II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

Your role will involve delivering clinical data management work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:
- Planning, coordination, and associated risk assessment of data review, via different tools and technologies.
- Defines the data review requirements for the trial with input to and from the RACT, in collaboration with the required Trial Partners.
- Collaborate with the relevant programmers to ensure setup of the data review tools.




- Maintains overview of the data review status and communicates relevant information to the CTDM.
- Collaborate with the relevant Trial Partners and other stakeholders to successfully achieve the data review deliverables on the trial
- Participation in process and toolkit improvement projects as required to support data review process evolution.
- Driving risk-based data management approaches to data review
- Data and issue trending relating to data quality and integrity and reporting of such to PoC.
- Liaising with process specialists on process changes and improvements
- Ensure that clinical data meets applicable regulatory requirements, quality, and data standards, and is reviewed and cleaned as per trial timelines.
- Ensure that DM-related activities comply with all applicable internal and external requirements.
- Provides input to Risk Assessment Categorization tool (RACT)
- Maintain a solid working relationship with the relevant DM trial partne

📌 Cdc II (Bengaluru)
🏢 IRE
📍 Bengaluru