Lead Clinical Data Science Programmer
India, Chennai
- Pay
- Pay not listed
- Work setting
- Not stated
- Employment
Full-time — employment source
Employment type in the employer’s listing: Full time
From the employer’s posting
What you’ll work on
Full postingLead design, development and validation of data science programming for trials
Program and validate datasets, tables, listings and figures (TLFs)
Write data specifications and analysis plans with biostatisticians and data managers
Run quality control and validation checks to keep clinical data accurate
Mentor junior programmers and give technical leadership to the team
From the employer’s posting
Leading the design, development, and validation of data science programming solutions for clinical trials.
Programming and validating datasets, tables, listings, and figures (TLFs) according to study requirements.
Collaborating with biostatisticians, data managers, and clinical teams to develop data specifications and analysis plans.
Ensuring the accuracy, consistency, and integrity of clinical data through rigorous quality control and validation checks.
Mentoring and guiding junior programmers and providing technical leadership within the data science programming team.
What you’ll bring
All qualificationsCore experience
- Bachelor's degree in life sciences, computer science, or a related discipline
- Excellent communication and leadership skills, with the ability to work collaboratively in cross-functional teams and manage multiple projects simultaneously.
Qualification wording
Bachelor's degree in life sciences, computer science, or a related discipline
Excellent communication and leadership skills, with the ability to work collaboratively in cross-functional teams and manage multiple projects simultaneously.
Education & alternatives
Required qualifications and experience: - Bachelor's degree in life sciences, computer science, or a related discipline - Years of Experience : 7+years
Tools in this posting
- R
- SAS
Source — Tool mentions in context
- Should have experience in SAS/JReview - Extensive experience in clinical data programming, with proficiency in SAS, R, or other relevant programming languages. - In-depth knowledge of clinical trial data structures, CDISC standards (SDTM, ADaM), and regulatory requirements.
- Must have experience in Rave/Veeva - Should have experience in SAS/JReview - Extensive experience in clinical data programming, with proficiency in SAS, R, or other relevant programming languages.
Posting record
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- Live
- First seen by us
- Oct 7, 2026 · 18 days ago
- Recorded sightings
- 69
- Last seen by us
- Oct 25, 2026
- Employer says posted
- Sep 9, 2026
These dates show when we found the listing. Check the employer’s website to confirm it is still accepting applications.
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Job description
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 Lead Clinical Data Science Programmer at ICON, you will design and develop clinical data solutions, ensuring the efficient handling, analysis, and reporting of complex clinical trial data.
What You Will Do:
You will manage day-to-day clinical data science activities, supporting your team to deliver quality outcomes.
Key responsibilities include:
- Leading the design, development, and validation of data science programming solutions for clinical trials.
- Collaborating with biostatisticians, data managers, and clinical teams to develop data specifications and analysis plans.
- Programming and validating datasets, tables, listings, and figures (TLFs) according to study requirements.
- Ensuring the accuracy, consistency, and integrity of clinical data through rigorous quality control and validation checks.
- Mentoring and guiding junior programmers and providing technical leadership within the data science programming team.
Your Profile:
You will have solid clinical data science experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
- Bachelor's degree in life sciences, computer science, or a related discipline
- Years of Experience : 7+years
- Must have experience in Rave/Veeva
- Should have experience in SAS/JReview
- Extensive experience in clinical data programming, with proficiency in SAS, R, or other relevant programming languages.
- In-depth knowledge of clinical trial data structures, CDISC standards (SDTM, ADaM), and regulatory requirements.
- Strong analytical and problem-solving skills, with a focus on data accuracy and quality.
- Excellent communication and leadership skills, with the ability to work collaboratively in cross-functional teams and manage multiple projects simultaneously.
- Willingness to travel as required (approximately 10%)
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
Source details
Source notes
Source excerptsSelected passages from the saved posting. Check the full description for conditions and exceptions.
- Pay
No pay amount identified in the saved description.
- Location & working pattern
India, Chennai
Working pattern and location restrictions need checking in the full posting.
- Work authorization
- Willingness to travel as required (approximately 10%) Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits
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