ICON is hiring for the position of Principal Clinical Data Standards Consultant in India. This is a senior-level opportunity for professionals with extensive experience in Clinical Data Standards, CDISC, CDASH, Controlled Terminology, Data Collection Standards, and Clinical Data Management.
The selected candidate will provide expert-level consulting and leadership in clinical data standards, support sponsors with standards implementation and governance, develop data standards libraries, and mentor junior professionals.
ICON Principal Clinical Data Standards Consultant – Job Overview
| Particulars | Details |
|---|---|
| Company | ICON |
| Position | Principal Clinical Data Standards Consultant |
| Job ID | JR153919 |
| Locations | Bengaluru / Chennai, India |
| Work Mode | Office or Home |
| Employment Type | Full-Time |
| Experience | 12–15 Years |
| Travel | Approximately 15% |
| Application Deadline | September 30, 2026 |
| Functional Area | Clinical Data Standards / Clinical Data Management |
About the Role
As a Principal Clinical Data Standards Consultant, the selected professional will provide expert-level knowledge in at least one clinical data standards domain.
The role involves developing and maintaining data standards libraries, supporting CDISC compliance, advising sponsors on standards implementation, participating in governance activities, and helping improve clinical data processes and technologies.
This is a senior consulting and leadership position requiring strong technical knowledge, business understanding, problem-solving ability, and communication skills.
Key Responsibilities
The selected candidate will be responsible for:
- Providing expert functional knowledge in at least one clinical data standards domain.
- Developing standards content for internal ICON projects and sponsor-facing engagements.
- Developing, implementing, and maintaining ICON Data Collection Standards Libraries.
- Ensuring data standards comply with CDISC, sponsor, and regulatory requirements.
- Acting as a subject matter expert for standards implementation and compliance.
- Identifying business challenges and recommending best practices.
- Supporting improvements to clinical data processes, products, and services.
- Collaborating with cross-functional teams to define data collection strategies.
- Participating in clinical data standards governance activities.
- Providing expert input on complex standards-related topics.
- Leading or contributing to departmental initiatives.
- Taking project lead responsibilities when required.
- Coordinating team members and project activities.
- Developing training materials and reference documentation.
- Supporting training related to CDASH and Controlled Terminology.
- Monitoring industry trends, regulatory developments, and emerging data standards.
- Supporting continuous improvement of ICON’s standards practices.
- Mentoring and guiding junior team members.
ICON Hiring for TMF Specialist I | Clinical Research Jobs in Chennai
Clinical Data Standards Responsibilities
The role also includes:
- Developing and implementing end-to-end data standards libraries from data collection through analysis.
- Providing internal and external consulting services on CDISC standards compliance.
- Supporting sponsors with development and implementation of data standards.
- Maintaining standards content and governance frameworks.
- Developing and delivering CDISC-related training.
- Supporting technologies used to implement clinical data standards.
- Participating in standards governance meetings.
- Providing expert standards input to assigned projects.
Required Experience
ICON is seeking professionals with:
12–15 years of relevant experience.
Candidates should have expert-level functional knowledge in at least one clinical data standards area.
Experience in clinical data standards, CDISC implementation, data collection standards, standards governance, or related clinical data management functions would be highly relevant.
Key Technical Skills
Candidates should have strong knowledge of areas such as:
- CDISC Standards
- CDASH
- Controlled Terminology
- Clinical Data Standards
- Data Collection Standards
- Standards Libraries
- Clinical Data Management
- Standards Implementation
- Standards Governance
- Regulatory Compliance
- Data Collection and Analysis
- Clinical Trial Data
Caidya Hiring Freshers for Trainee Statistical Programming | Clinical SAS Jobs
Leadership and Consulting Skills
The successful candidate should be capable of:
- Leading complex standards-related initiatives.
- Solving complex clinical data problems.
- Providing expert recommendations to internal teams and sponsors.
- Mentoring junior team members.
- Coordinating project teams.
- Presenting complex technical information clearly.
- Influencing stakeholders and securing agreement on complex matters.
- Working effectively with cross-functional and international teams.
Problem-Solving Responsibilities
This is a senior-level position requiring the ability to:
- Analyze complex clinical data standards problems.
- Apply sophisticated analytical thinking.
- Develop innovative solutions.
- Identify opportunities for process improvement.
- Recommend best practices based on business requirements.
- Ensure quality and compliance standards are maintained.
Travel Requirement
The position may require approximately 15% domestic and/or international travel.
Work Location
The position is available in:
- Bengaluru, India
- Chennai, India
Work Mode: Office or Home
The exact working arrangement may depend on project and business requirements.
Salary and Benefits
ICON has not disclosed a specific salary range for this position in the supplied job description.
The company states that its rewards package may include:
- Competitive base salary
- Performance-related incentives
- Health and wellbeing programs
- Medical benefits where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programs
- Learning and development opportunities
- Structured training and career development programs
Benefits may vary depending on the role and location.
Who Should Apply?
This opportunity is best suited for experienced professionals with:
- 12–15 years of relevant experience
- Expert knowledge of at least one clinical data standards domain
- Strong CDISC knowledge
- Experience with CDASH and Controlled Terminology
- Clinical data standards implementation experience
- Standards governance experience
- Sponsor consulting experience
- Strong leadership and mentoring capabilities
- Excellent communication and presentation skills
- Ability to solve complex problems independently
Application Deadline
Last Date to Apply: September 30, 2026
Candidates interested in this senior-level Clinical Data Standards Consultant opportunity should submit their application before the stated deadline.
How to Apply
Interested and eligible candidates can apply online through the official ICON careers portal for Principal Clinical Data Standards Consultant – Job ID JR153919.
Candidates should ensure their resume clearly highlights their experience in CDISC, CDASH, Controlled Terminology, clinical data standards, standards libraries, data governance, sponsor consulting, and clinical data management.
