ICON Hiring Clinical Data Coordinator I (CDC I) - Bangalore, Chennai & Trivandrum
Are you seeking high-paying ICON Clinical Data Coordinator Jobs or Clinical Data Management Careers in Bangalore, Chennai, and Trivandrum? The globally recognized contract research organization (CRO), ICON Plc, has announced recruitment for Clinical Data Coordinator I (CDC I).
This role is ideal for freshers or early-career professionals from pharmacy, biotechnology, or life sciences background who want to build a career in data verification, database specifications, eCRF review, and clinical study data workflows. To learn the best strategies to apply, read our detailed tutorial on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particulars | Details |
|---|---|
| Position | Clinical Data Coordinator I (CDC I) |
| Company | ICON Plc (Clinical Research Services) |
| Job Requisition ID | JR153061 |
| Location | Bangalore, Chennai, Trivandrum (India) |
| Employment Type | Full-Time |
| Work Mode | Office with Flex (Hybrid) |
| Experience Required | Basic knowledge of Clinical Data Management (0–2 Years) |
| Qualifications | Bachelor's Degree in Life Sciences or Healthcare |
| Application Deadline | Apply Immediately (Not Mentioned) |
💼 Key Responsibilities
- Assist the Data Management Study Lead in the design and development of eCRF, data validation edit specifications, and study-specific procedures.
- Review clinical databases, patient records, and third-party data inputs in accordance with the study data review plans.
- Identify data discrepancies and issue clear, accurate, and concise queries to investigator sites for resolution.
- Perform database reviews and dispatch queries to ensure that project timelines and milestones are met.
- Fulfill documentation tasks, including filing, managing, and archiving clinical study documentation in the study master file.
- Collaborate actively with clinical data scientists, biostatisticians, and clinical trial coordinators.
Clinical data coordinator roles require a strong understanding of data indexing, validation, and analytics. To check how clinical data coordinator positions compare with clinical SAS programming, read our detailed comparison on Clinical SAS vs Clinical Data Management.
🎓 Qualifications & Eligibility Criteria
Candidates possessing the following qualifications are eligible to apply:
- Degree: Bachelor's degree in a relevant healthcare or biological field, such as Pharmacy, Biotechnology, Biochemistry, Microbiology, or general Life Sciences.
- Core Skills: Basic knowledge of clinical data management workflows within the pharmaceutical or contract research (CRO) industry.
- Software: Familiarity with clinical database software and platforms (e.g., Medidata Rave, Oracle RDC, Inform, or similar Electronic Data Capture systems).
For pharmacy and life sciences graduates looking to evaluate their long-term path, read our salary and career guide on B.Pharm Careers: India vs USA.
Required Soft Skills
- Strong attention to detail with the capability to identify small errors in large scientific datasets.
- Excellent written and verbal communication skills in English (critical for issuing queries to global sites).
- Willingness to collaborate and work effectively in a team environment with strict timelines.
- Basic knowledge of global regulatory guidelines (e.g., ICH-GCP) is a plus.
💰 Rewards & Benefits
ICON Plc offers a comprehensive total rewards package, which includes:
- Competitive base salary and performance-linked incentives.
- Comprehensive medical, dental, and vision insurance coverage.
- Retirement and pension plan contributions.
- Life assurance and disability insurance programs.
- Structured learning resources and clear internal career pathways.
To learn about typical roles involved in clinical trial operations and documentation, check our comprehensive Clinical Research Coordinator (CRC) Guide.
🌟 Why Join ICON?
- ICON is a leading global clinical research partner delivering key insights to drug developers.
- Work with a collaborative, values-driven culture emphasizing integrity, agility, and inclusion.
- Develop expertise in advanced Electronic Data Capture (EDC) systems used in global clinical trials.
If you want to compare clinical operations with technology consulting careers, check our analysis on Healthcare IT vs Clinical Healthcare.
📑 Resume Tips for ICON
- Highlight any exposure or training in EDC databases like Medidata Rave or Oracle RDC.
- Explicitly mention your knowledge of clinical trial phases, ICH-GCP guidelines, and data validation edit checks.
- Ensure your CV is clean, highly structured, and optimized for ATS systems.
🎯 ICON CDC I Interview Questions
- What is an eCRF and what is its role in clinical data management?
- Explain the process of query lifecycle (opening, answering, closing queries).
- What is the purpose of edit check specifications in clinical database validation?
- How do you ensure data security and protocol compliance when reviewing clinical trial data?
- Describe a scenario where you had to work under tight timelines to complete a review.
📌 How to Apply?
Eligible candidates can apply online directly through ICON's Workday recruitment portal using the link below. Since no specific application deadline is mentioned, candidates are advised to apply immediately before the link closes. To optimize your registration profile, read our tutorial on how to apply for healthcare and pharma jobs online.
🚀 Apply Now
Apply Online❓ Frequently Asked Questions
Q. What is the application deadline?
No deadline is mentioned in the official post. Candidates should apply immediately.
Q. Who is eligible for this role?
Bachelor's degree graduates in Life Sciences or Healthcare fields with basic knowledge of Clinical Data Management.
Q. What is the work model and locations?
The role is full-time, hybrid (office with flex), based in Bangalore, Chennai, or Trivandrum.
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