.png?v=4006b31bba9e99f4b0269f7fc517855e)
A Day in the Life of a Clinical Data Science Programmer
A Day in the Life of a Senior Lead Clinical Data Science Programmer
In the ever-evolving world of clinical research, professionals with specialized technical skills play a crucial role in advancing healthcare innovations. Today, we're spotlighting Punitha Margaret, a Senior Lead Clinical Data Science Programmer at ICON's Chennai office, who shares her professional journey and experiences that have shaped her career in clinical data science.
A Journey of Growth
Punitha has been with ICON for over a year, but her career path demonstrates the diverse opportunities available within the clinical research industry. Starting as a Senior Report Programmer, she was deeply involved in creating, validating, and maintaining clinical trial reports - establishing the foundation for her expertise in clinical data management.
"I've always had a strong passion for programming and the intersection of data science with real-world applications," Punitha reflects. "Early in my career, I recognized the profound impact that accurate data and clear reporting can have on the development of new treatments and improving patient outcomes." Her dedication and skills soon led to a promotion to Principal Report Programmer, where she took on greater responsibility, overseeing more complex programming tasks and automations.Expanding Beyond Technical Boundaries
Not content with limiting herself to technical roles, Punitha sought to broaden her understanding of clinical processes. This ambition led her to transition into the role of Senior Business Analyst, where she applied her technical background to more strategic responsibilities.
"As I progressed, I discovered how much I enjoyed the unique challenges of programming and reporting in clinical trials, particularly in ensuring data integrity, efficiency, and the clarity of reports," she says. In her current position as Senior Lead Clinical Data Science Programmer, Punitha leads teams of programmers, manages complex projects, and oversees the creation of clinical trial reports from inception to completion. Her responsibilities include ensuring accuracy, integrity, and regulatory compliance of clinical data while mentoring junior and senior team members.Professional Development at ICON
When asked about how ICON supports her professional development, Punitha highlights the company's approach to role diversification.
"ICON offers valuable opportunities for role diversification, which is crucial for my professional development. This approach allows me to take on different roles within the company, broadening my skill set and providing a well-rounded understanding of how the organisation operates."Punitha also appreciates ICON's investment in continued learning through access to conferences, industry events, and internal networking opportunities. These resources help her expand her professional connections and gain valuable perspectives from others in the industry.Work-Life Balance and Supportive Culture
Beyond career growth, Punitha values the quality of life that working at ICON provides.
"What keeps me at ICON is the excellent work-life balance and the supportive work culture. The flexibility allows me to maintain a healthy personal life while staying productive and engaged at work." She emphasizes that ICON's positive, inclusive culture fosters a sense of belonging, making it easy to stay motivated and committed to her work - essential factors for long-term career satisfaction in the demanding field of clinical research.The Passion Behind the Profession
At the heart of Punitha's career is a genuine passion for the work she does. "I enjoy problem-solving, managing large datasets, and mentoring others to improve their skills, all while contributing to critical research that can directly affect patient lives," she explains.
This combination of technical expertise, leadership skills, and commitment to improving healthcare outcomes through data exemplifies the type of professionals who thrive at ICON Clinical Research.Sign up for post alerts
ICON & You
The potential of together.
Careers that improve the lives of patients, our clients and each other. Are you ready to make a difference?
View jobsRelated jobs at ICON
Salary
Location
India, Chennai
Department
Full Service - Corporate Support
Location
Chennai
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Accounting & Finance
Job Type
Permanent
Description
The Role We are looking for a candidate who can Build Report & Analyse financial results to leaders in the context of each Business unit objective.This person is also responsible for Owing P &L, Forec
Reference
JR129051
Expiry date
01/01/0001
Author
Puja JaiswalAuthor
Puja JaiswalSalary
Location
Bangalore
Department
Biometrics Roles
Location
Bangalore
Business Area
ICON Strategic Solutions
Job Categories
Biometrics Portfolio
Job Type
Permanent
Description
The role involves being a Senior Lead clinical data science programmer in the Clinical Data Management area, focusing on enhancing data review and cleaning processes with innovative reports. It entail
Reference
2025-118056
Expiry date
01/01/0001
Author
Abhisikta MishraAuthor
Abhisikta MishraSalary
Location
Romania, Bucharest
Location
Sofia
Warsaw
Bucharest
Remote Working
Hybrid: Office/Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Contracts Administration
Job Type
Permanent
Description
Responsible for the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, and other ancillary agreements with study sites.Responsibilities:Drafts, reviews,
Reference
JR129348
Expiry date
01/01/0001
Author
Magda KozuszekAuthor
Magda KozuszekSalary
Location
India, Chennai
Location
Chennai
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Accounting & Finance
Job Type
Permanent
Description
We are currently seeking an IPG Reporting Analyst to join our diverse and dynamic team. As an IPG Reporting Analyst at ICON, you will play a crucial role in supporting the management and analysis of I
Reference
JR129208
Expiry date
01/01/0001
Author
Puja JaiswalAuthor
Puja JaiswalRelated stories
.png)
Teaser label
IndustryContent type
BlogsPublish date
05/05/2025
Summary
Navigating Regulatory Landscapes: Comparing FDA, EMA, & MHRA in Clinical Trials In clinical research, no matter how promising a new therapy may be, it will go nowhere without regulatory appro
.png)
Teaser label
IndustryContent type
BlogsPublish date
04/22/2025
Summary
What is an IND or NDA? A Guide for Aspiring Clinical Research Professionals If you’re considering a career in clinical research or the broader pharmaceutical and biotech industry, you’ve likely c
.png)
Teaser label
IndustryContent type
BlogsPublish date
04/22/2025
Summary
When it comes to clinical trials, one of the most important documents you’ll hear about is the Informed Consent Form (ICF). Whether you're starting out in clinical research or exploring job opportunit
Recently viewed jobs
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON