Back to list

Vacancy description

Principal Clinical Data Standards Consultant in Bangalore, भारत

ICON plc

  • RemoteWork from anywhere

Bangalore, भारत

Prinicipal Clinical Data Standards Consultant

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Principal Clinical Data Standards Consultant 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 focus will be on coordinating consulting and advisory services delivery, resolving issues, and developing team capability.

Key responsibilities include:
  • As a Senior Clinical Data Standards Consultant at ICON Plc, you will be responsible for:
  • Developing tools to aid in the implementation and compliance of CDISC, Sponsor, and ICON standards.
  • Collaborating with cross-functional teams to define data collection strategies and standards for clinical trials.
  • Developing and maintaining training and reference materials related to standards topics including CDASH, SDTM, Terminology, ADaM, define-XML and regulatory submission requirements.
  • Managing the development and maintenance of data management processes and tools.
  • Keeping abreast of industry trends and regulatory updates related to data standards and ensuring their integration into ICON's practices.

Your Profile:

You will have solid consulting and advisory services experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:
  • To excel in this role, you should possess the following qualifications and attributes:
  • Bachelor's degree in life sciences, computer science, or a related discipline
  • SDTM expert with a background that includes programming in SAS, R and other languages. 
  • Should have a minimum of 8 years experience in the industry in roles that demonstrate the knowledge and skill in the above. 
  • Statistical programming role focused on SDTM tasks. 
  • Should demonstrate leadership skills
  • Extensive experience in clinical data management and standards within the pharmaceutical or biotechnology industry.
  • Advanced Proficiency in CDISC (Clinical Data Interchange Standards Consortium) standards and relevant regulations (e.g., FDA, EMA).
  • Excellent analytical and problem-solving skills with a keen attention to detail.
  • Excellent communication and collaboration abilities to work effectively in cross-functional teams.
  • Willingness to travel as required (approximately 15%)

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

Similar vacancies

More like this role

Principal Clinical Data Standards Consultant at ICON, a global clinical research organization. Design and analyze clinical trials, lead data standards implementation across teams, and ensure compliance with CDISC and regulatory requirements. Based in Bangalore, India. Responsibilities - Coordinate consulting and advisory ...

Bangalore, भारत

Senior Clinical Data Coordinator role at ICON involves designing and analyzing clinical trials while managing complex medical data. The position requires leading data management initiatives, ensuring regulatory compliance, and mentoring junior coordinators in a sponsor-dedicated model. Responsibilities - Design and maintain ...

Chennai, भारत

  • Remote
  • Hybrid
  • On-site
... 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, ...

Thiruvananthapuram, भारत

  • Contract
  • Data Science
... phase I to IV clinical studies in Novartis Global Development Organization. - Co-ordinate activities of Data Managers either internally or externally. - Make data Mgmt decisions and propose strategies at study or project level. - Ensure application of consistent data Mgmt processes, influence increased standardization and ...

Hyderabad, भारत

Senior Principal Architect, EDT Data Architecture Strategy & Standards The Senior Architect, Data & Analytics Architecture owns the enterprise data and analytics architecture strategy, standards, and design patterns for the global Azure/Databricks Lakehouse ecosystem. Actively shapes architectural and technical decisions ...

Gurgaon, भारत

  • Full-time
Senior Principal Architect, EDT Data Architecture Strategy & Standards The Senior Architect, Data & Analytics Architecture owns the enterprise data and analytics architecture strategy, standards, and design patterns for the global Azure/Databricks Lakehouse ecosystem. Actively shapes architectural and technical decisions ...

Gurgaon, भारत

Stryker seeks a Senior Principal Architect to define enterprise data and analytics strategy, standards, and design patterns across a global Azure/Databricks Lakehouse ecosystem. This player-coach role combines hands-on architectural leadership with design authority oversight and direct engagement in solution delivery. Responsibilities ...

Gurgaon, भारत

  • Hybrid
  • Data Analytics
... technical leadership could transform how clinical trial risks are detected and managed? As Principal Solution Architect, Clinical Data Analytics & Technology ( RBQM Data Analyst), you will design and deliver scalable central monitoring analytics and technology solutions that strengthen clinical data quality, trial oversight, and ...

Hyderabad, भारत

  • Data Science
... to maintain data quality and trial readiness. Responsibilities - Oversee all Clinical Data and Information Sciences activities and deliverables for assigned clinical trials - Lead and provide direction to Data Managers; ensure regulatory and procedural compliance - Establish data acquisition standards, quality risk indicators, ...

Chennai, भारत

  • Full-time
  • Contract
... • With Minimal guidance - support, overview of validation of new Device integrations. • Oversight & Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor. • Ensure that all the deliverables are of expected quality standards and meet customer expectations. • With guidance, ...

Thana, भारत