CDC IIAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a CDC II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of creative 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:
- Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.
- Manage clinical and third-party data reconciliation based on edit specifications and data review plans.
- Tracks and communicates status of study and task metrics to clinical data scientist, project team, and functional management.




- Address data related questions and recommend potential solutions.
- Identify root cause to systematically resolve data issues.

Your Profile:
You will bring relevant clinical data management experience, along with the following qualifications and skills.

Required qualifications and experience:
- Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.
- Intermediate knowledge of clinical data management within the pharmaceutical or biotechnology industry.
- Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).
- Strong attention to detail and the ability to work effectively in a fast-paced environment.
- Excellent communication skills and the ability to collaborate with cross-functional teams.
- Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.

Employment with ICON is contingent upon having the legal right to work in the c

📌 Cdc II (Bengaluru)
🏢 IRE
📍 Bengaluru