Senior Clinical Data Coordinator

ICON Strategic Solutions; Chennai; Hybride; INR 600 000 - 1 200 000; Plein temps

Résumé du poste

ICON Strategic Solutions in Chennai, India is seeking a Senior Clinical Data Coordinator to join in an office-based or home-based capacity. You will design and analyse clinical trial data, ensuring high data quality and regulatory compliance to support patient-centric treatments worldwide.

You will lead on data management tasks with a focus on quality, collaborate with clinical operations and biostatistics, and mentor junior coordinators.

Qualifications

• Bachelor's degree in Life Sciences or Healthcare.

Responsabilités

• Create and maintain data management plans and documentation in line with regulatory standards.
• Identify and resolve data discrepancies to improve data quality throughout study lifecycle.
• Collaborate with clinical operations and biostatistics to implement data management strategies.
• Support study timelines including filing/archiving documentation and querying sites.
• Mentor junior data coordinators on reconciliation, coding and cleaning procedures.

Connaissances

Clinical data management

Data quality & reconciliation

Cross-functional collaboration

Attention to detail

Regulatory awareness (ICH-GCP)

Travel willingness

Formation

Bachelor's degree in Life Sciences or Healthcare

Outils

Medidata

Oracle RDC

Description du poste

Senior Clinical Data Coordinator - Office based or Home based

At 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 Senior CDC 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

You will lead on clinical research tasks requiring technical depth, with a focus on quality and continuous improvement.

Key Responsibilities Include

• Create and maintain detailed data management plans and documentation, ensuring compliance with industry standards and regulatory requirements.
• Participate in the identification and resolution of data discrepancies and issues, working to streamline data flow and enhance data quality throughout the study lifecycle.
• Collaborate closely with cross-functional teams, including clinical operations and biostatistics, to develop and execute data management strategies tailored to specific studies.
• 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.).
• Mentor junior data coordinators, providing expert guidance on data reconciliation, coding, and cleaning procedures.

Your Profile

You will have a strong foundation in clinical research, with the experience to work independently and guide others.

Required Qualifications And Experience

• Bachelor’s degree in a relevant field, such as Life Sciences or Healthcare.
• Proven experience in 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.
• Willingness to travel as required (approximately 5%)

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.