ICON
CDC II
Bangalore, Bengaluru
- Remote
- Full-time
- Location
- Posted 14 May 2026
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... CDC II job in India, Bangalore | ICON JUMP TO CONTENT Manage your application Shortlist 0 Search Careers in ICON Careers We encourage our people to seize the opportunity to bring flexibility, innovation and determination to every situation. By doing this, our people build exciting and rewarding careers, deliver results to help bring life-changing medicines and devices to market and maintain ICON’s success as an industry leader. View jobs at ICON About Icon Overview of Service Lines Job Categories ICON Full Service Full Service Full-service roles offer the opportunity to work on projects and programmes on behalf of the world’s most innovative pharma, biotech and medical device companies. 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View roles Recruitment Process Inside ICON About ICON Our Culture & Our People Our Mission & Values Overview of Service Lines Full Service Strategic Solutions (FSP) Global Business Services Accellacare Site Network ICON Biotech ICON Leadership Our Locations Our Locations With headquarters in Dublin, Ireland, ICON has employees in 119 locations across 53 countries. View roles Global Office Locator Ireland Asia Pacific Australia China India Japan Korea Malaysia Taiwan Europe, Middle East & Africa Belgium Bulgaria Germany Hungary Italy Netherlands Poland Romania Slovakia South Africa Spain Türkiye United Kingdom United States Latin America Argentina Brazil Chile Colombia Mexico Global Office Locator Why ICON? Why ICON? No matter what part of ICON you work in, you are contributing to solving some of the most complex healthcare challenges and are helping to deliver new medicines and devices that are impacting millions of peoples’ lives, right across the world. Find out more about life at ICON Inclusion & Belonging ICON Cares - ESG Rewards & Benefits Learning & Development Development Opportunities CRA Learning Opportunities Career Journeys Our Culture & Our People Inclusion & Belonging PRIDE SPACE IGNITE embRACE DAWN SERVE ICON Cares - Environment, Social and Governance US Veteran Community Awards Blogs Events Events? full service mean for you? Integer posuere erat a ante venenatis dapibus posuere velit aliquet. Duis mollis, est non commodo luctus, nisi erat porttitor ligula. Read more Early Talent Early Talent Early talent programs are designed to provide participants with opportunities to gain valuable experience, develop their skills, and build relationships with experienced leaders within the organization. Early talent programs can take many forms, including internships, academy programs, and leadership development programs. ICON is committed to recruiting top talent while also fostering a culture of learning and development within the organization. Building a Successful Clinical Research Resume Landing Your First Job in Clinical Research Internships Graduate Opportunities Hints & Tips for Graduates graduate What does full service mean for you? Integer posuere erat a ante venenatis dapibus posuere velit aliquet. Duis mollis, est non commodo luctus, nisi erat porttitor ligula. Read more Career Resources Our Culture Application Process AI Usage Policy Our Mission & Values CDC II Location: Bangalore, Bengaluru Reference: JR150695 Categories Clinical Data Management __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions (FSP) __vacancyopjusttionswidget.opt-Remote Working __ Hybrid About the role This vacancy has now expired. Please click here to view live vacancies. CDC II ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. 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: Review clinical data in various database formats, datasets, listings, reports, visualizations, and analytics for completeness, accuracy, and integrity. Raise, review and close of queries with EDC/CDMS ensuring that data is reviewed and corrected as required by qualified site staff. Working closely with the DM trial partners and provide support as required to additional Data Management activities. Follow the Data Management Monitoring (DMM) and Risk Assessment Categorisation Tool (RACT) on a trial. Planning, coordinating, and assessing the associated risks of data review using various tools and technologies. Support the creation and execution of data review related reports and data review strategy. Maintaining an overview of the data review status and communicating relevant information to the DM Trial Partners. Maintaining an overview of the data review status and communicating relevant information to the DM Trial Partners. Collaborating with relevant Trial Partners and other stakeholders to successfully achieve the data review deliverables on the trial. The CDIA may assume the Clinical Trial Data Manager (CTDM) role for the clinical trial(s). Effectively communicate data findings including visualizations with clear explanations. Proactively own and independently drive all data review under experienced CDR purview, taking complete ownership and responsibility. Use data visualisation methods to review and understand data to support trial partners in making operational decisions. Maintain CDR relevant trial documentation and ensure applicable archival on an ongoing basis. Resolves or escalates issues identified during the review and update to DM trial partners. Prepare and participate in audits and inspections. 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. 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 maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. 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, color, 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 or submit a request here 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. Are you a current ICON Employee? Please click here to apply Share: Hi, I am Jypson and I manage this role Talent Sourcing Recruiter Icon Strategic Solutions View my profile Email [email protected] View my other roles Send me a message First Name * Last Name * Email address * Enquiry * Send Cancel Get Job Alerts! Sign up to receive job updates tailored to your interests. Sign Up Not Ready to Apply? Join our Talent Community for future alerts. Sign up Explore more about ICON About ICON Explore Global Office Locator Explore Benefits & Rewards Explore Inclusion & Belonging Explore Career Pathways Explore Environmental, Social & Governance Explore List #1 Day in the life From Clinical Trial Assistant to Clinical Operations Manager Teaser label A Day In The Life Content type Blogs Publish date 04/21/2023 Summary From Clinical Trial Assistant to Clinical Operations Manager, Adrienne Purdy shares her journey. I have been at ICON since 2013 and I have been growing my career here from the ground up. I star Teaser label Adrienne Purdy shares her career journey and experience at ICON. Read more by Adrienne Purdy by Adrienne Purdy Sam’s career journey from trainee CRA to Clinical Trial Manager Teaser label Our People Content type Blogs Publish date 12/22/2022 Summary If there's one thing that the pandemic made clear, it was that clinical research was an essential part of the global recovery and protecting us from future pandemics. Being one of the most cri Teaser label If there's one thing that the pandemic made clear, it was that clinical research was an essential part of the global recovery. 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