Clinical Data Programmer

3 days ago


Chennai, India ICON Full time

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.

Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

INSERT ADVERT TEXT HERE

**Benefits of Working in ICON**:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and 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.



  • Chennai, India ICON Full time

    At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...


  • Chennai, Tamil Nadu, India ICON Plc Full time

    Clinical Data Science Programmer - Office based - Chennai/ Trivandrum ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a...


  • Chennai, India ICON Full time

    At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...

  • Associate Programmer

    2 weeks ago


    Chennai, Tamil Nadu, India IQVIA Full time ₹ 2,00,000 - ₹ 8,00,000 per year

    Associate Programmer Job Overview Provide technical assistance as part of a team to develop and maintain clinical systems that meet internal and external clients' needs. Assist with the development of database for local, regional, or transnational use. Essential Functions • Assist in planning and coordinating database design, development,...


  • Chennai, Tamil Nadu, India Sportism Full time ₹ 5,00,000 - ₹ 12,00,000 per year

    Position OverviewWe are seeking an experienced Clinical Data Specialist II to join our clinical research team in Chennai. The successful candidate will be responsible for accurate and timely data entry into Electronic Data Capture (EDC) systems from various e-source documents, including real-time data and Clinical Research Information Officer (CRIO) sources....


  • Chennai, Tamil Nadu, India Insys IT Full time ₹ 3,00,000 - ₹ 4,00,000 per year

    Job descriptionRole & responsibilities:Overseeing the collection, validation and processing of clinical trial data.Developing and implementing data management procedures for clinical trials.Supporting and facilitating the review of medical coding for validity and completeness.Ensuring compliance with applicable regulations, protocols and standard operating...


  • Chennai, India Pfizer Full time

    Hands on programming role, supporting deliverables in the study/project/portfolio/standards team, of less or medium complex statistical programming deliverables - Mentored/Guided by Senior Statistical Programmers within Standards/Study/ Project/ Portfolio/ TA’s - Collaborate with Senior Programmers/Leads and complete the assigned tasks - Ensures adherence...


  • Chennai, Tamil Nadu, India Allucent Full time ₹ 8,00,000 - ₹ 12,00,000 per year

    At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Senior Clinical Data Manager I to join our A-team.The Senior Clinical Data Manager I (SrCDM1) is responsible for leading data...


  • Chennai, Hyderabad, India Agilisium Full time ₹ 8,00,000 - ₹ 12,00,000 per year

    Responsible for gathering, analyzing, and interpreting clinical and operational data to inform strategic business decisions.This role supports the efficiency and effectiveness of clinical operations by developing reports, dashboards, and key performance indicators (KPIs) to track performance, identify trends, and drive improvements in quality, cost, and...


  • Chennai, India HCLTech Full time

    Key Responsibilities:Bachelor’s degree in Life Sciences, Computer Science, or related field.8+ years of experience in clinical data testing and validation.Perform UAT for CRF screens, database edit checks, and exceptional reports/listings.Test clinical study setup configurations including protocol parameters, visit schedules, and form designs.Validate...