Senior Clinical Data Coordinator Openings at ICON plc

ICON Strategic Solutions Hiring Clinical Data Coordinator II – Clinical Data Management Jobs in Chennai

The global clinical research organization ICON Strategic Solutions is inviting applications for the position of Clinical Data Coordinator II within the Clinical Data Management department. This opportunity is based in Chennai and follows a hybrid work model. The vacancy is ideal for professionals with strong experience in clinical research data management, medical data analysis, and pharmaceutical clinical trials. Candidates with a Life Sciences or healthcare background and experience working with electronic clinical data systems are encouraged to apply for this growing role in the CRO industry.

Company Overview

ICON Strategic Solutions, a division of ICON plc, is a globally recognized healthcare intelligence and clinical research organization. The company partners with pharmaceutical, biotechnology, and medical device companies to accelerate the development of innovative therapies and life‑saving treatments.

With a strong presence across multiple countries, ICON supports the full spectrum of clinical trial services including clinical development, regulatory consulting, data management, and biostatistics. The organization is widely respected for maintaining high scientific standards, regulatory compliance, and operational excellence in global clinical research programs.

By joining ICON Strategic Solutions, professionals gain exposure to advanced clinical trial technologies, global pharmaceutical projects, and data-driven healthcare innovation that directly contributes to the advancement of modern medicine.

Job Role and Responsibilities

The Clinical Data Coordinator II will play a critical role in managing and validating clinical trial data to ensure accuracy, compliance, and regulatory readiness. The role requires close collaboration with clinical data scientists, project teams, and cross‑functional research teams to maintain high‑quality clinical data management standards.

Key responsibilities include:

• Assist the Data Management Study Lead in maintaining electronic Case Report Forms (eCRF) and study documentation.
• Support the development and maintenance of Data Validation Specifications and study‑specific data management procedures.
• Perform reconciliation of clinical trial data and third‑party vendor data according to defined edit specifications.
• Monitor and track clinical data management metrics and communicate updates to project stakeholders.
• Investigate and resolve data discrepancies within clinical trial databases.
• Identify root causes of data issues and implement systematic corrective solutions.
• Ensure that clinical research data follows regulatory standards and Good Clinical Practice guidelines.
• Collaborate with cross‑functional teams including clinical operations, biostatistics, and regulatory affairs.

This position requires strong analytical thinking, attention to detail, and the ability to work within fast‑paced clinical development environments.

Eligibility and Qualifications

Candidates interested in applying for the Clinical Data Coordinator II role should meet the following eligibility criteria:

Educational Qualification:
Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Biochemistry, Microbiology, Clinical Research, Healthcare Sciences, Biomedical Sciences, or related disciplines.

Experience:
• Minimum 5 years of experience in Clinical Data Management within the pharmaceutical, biotechnology, or CRO industry.

Required Skills:

• Working knowledge of clinical data management systems such as Medidata Rave, Oracle RDC, or similar electronic data capture platforms.
• Understanding of clinical trial data standards and regulatory requirements including ICH‑GCP guidelines.
• Strong analytical and data review capabilities in clinical trial datasets.
• Excellent communication and teamwork skills to collaborate with global clinical research teams.
• Ability to handle complex medical datasets while maintaining high data integrity.

Professionals with experience in clinical trials, pharmaceutical research data management, and healthcare analytics will find this role particularly suitable for career growth in the clinical research industry.

Location and Work Model

Location: Chennai, India

Work Model: Hybrid work environment allowing a balance between office collaboration and flexible work arrangements.

Salary: Competitive salary package aligned with industry standards and candidate experience.

ICON also offers comprehensive employee benefits designed to support professional growth and work‑life balance.

Employee Benefits

ICON Strategic Solutions offers a competitive benefits package designed to support employee well‑being and long‑term career development.

Benefits may include:

• Competitive salary structure within the clinical research industry
• Health insurance plans for employees and family members
• Retirement planning and financial savings programs
• Global Employee Assistance Program supporting mental health and well‑being
• Flexible work arrangements and work‑life balance initiatives
• Paid annual leave and wellness benefits
• Optional benefits such as childcare vouchers, travel subsidies, gym membership discounts, and health assessments

These benefits make ICON one of the most preferred employers in the global CRO and pharmaceutical research sector.

Application Process

Candidates interested in applying for this clinical research job opportunity can submit their application through the official ICON careers portal.

Apply Here:
https://careers.iconplc.com/job/clinical-data-coordinator-in-india-chennai-jid-47687

Applicants are encouraged to apply even if they are unsure about meeting every requirement, as ICON values diverse experiences and skills.

Frequently Asked Questions

What does a Clinical Data Coordinator do?

A Clinical Data Coordinator manages clinical trial datasets, ensures data accuracy, validates patient information, and supports clinical research teams in maintaining compliant and high‑quality research databases.

Who can apply for this clinical research job?

Candidates with a bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, Biochemistry, Microbiology, or related healthcare disciplines with relevant clinical data management experience can apply.

What software knowledge is useful for this role?

Experience with clinical data management platforms such as Medidata Rave, Oracle RDC, or other electronic data capture systems is valuable for this position.

Is this role suitable for freshers?

No. This position requires approximately five years of experience in clinical data management within the pharmaceutical or CRO industry.

Where is the job located?

The role is based in Chennai, India, with a hybrid working model.

Job Summary

Category	Details
Company	ICON Strategic Solutions
Vacancies	Clinical Data Coordinator II
Required Education	Life Sciences, Pharmacy, Biotechnology, Biochemistry, Microbiology, Clinical Research, Healthcare Sciences, Biomedical Sciences
Experience	Minimum 5 years in Clinical Data Management

Tagged as: Pharma Jobs in Bangalore