Are you a life sciences graduate dreaming of building a career in the pharmaceutical or CRO industry? Do you have a keen interest in Clinical SAS programming, R programming, and clinical data standards? If yes, this opportunity in Hyderabad might be your perfect starting point!
A fast-growing clinical research organization, Panakeia Clinical Services LLP, is inviting applications from freshers and early-career professionals (0–2 years of experience) who want to establish themselves in the field of Clinical Programming.
Let’s explore why this opportunity could be a major step forward in your career journey. 🌱
🌟 Why Choose a Career in Clinical SAS & R?
The pharmaceutical and CRO industries are rapidly evolving, and clinical data analysis plays a critical role in drug development and regulatory approvals. Clinical programmers work closely with biostatisticians and clinical teams to transform raw clinical trial data into meaningful insights.
Here’s why Clinical SAS & R is a powerful career choice:
✔️ High demand across pharmaceutical and CRO companies
✔️ Opportunities to work on global clinical trials
✔️ Strong salary growth potential
✔️ Long-term career stability
✔️ Exposure to international regulatory standards
If you enjoy working with data, statistics, and structured systems, Clinical Programming can be both intellectually rewarding and financially promising. 📊💼
📍 About the Opportunity
Location: Hyderabad
Eligibility: B.Sc. / M.Sc. Graduates
Experience: 0–2 Years
Industry: Pharma / CRO
This opportunity is ideal for:
- Fresh graduates eager to enter the clinical research domain
- Professionals with foundational SAS or R knowledge
- Candidates looking to transition into Clinical Programming
- Individuals committed to continuous learning and quality standards
🧠 Key Skills Required
To succeed in this role, candidates should have knowledge or training in:
📌 SDTM & ADaM Dataset Creation and Validation
Understanding how to structure clinical trial data using standardized models is crucial. SDTM (Study Data Tabulation Model) and ADaM (Analysis Data Model) ensure regulatory compliance and efficient data analysis.
📌 TFL Outputs & Statistical Reporting
Clinical programmers generate Tables, Figures, and Listings (TFLs) that support statistical analysis and clinical study reports.
📌 CDISC Standards
Knowledge of Clinical Data Interchange Standards Consortium guidelines ensures data meets global regulatory expectations.
📌 SAS & R Programming
Hands-on exposure to SAS and/or R for data cleaning, transformation, and reporting is highly valuable.
📌 Quality & Compliance Mindset
Accuracy, documentation practices, and validation are critical in clinical research environments.
If you are passionate about structured data, programming logic, and precision, this role aligns perfectly with your skill set. 💻✨
🎯 What Makes This Opportunity Special?
Working with Panakeia Clinical Services LLP offers more than just a job—it provides a platform to grow.
🌱 Real-Time Industry Projects
You’ll gain exposure to practical clinical datasets and regulatory workflows.
👩🏫 Mentor-Led Guidance
Early-career professionals benefit from structured mentorship and hands-on training.
🚀 Startup Growth Environment
Being part of an innovative CRO startup allows you to learn faster, take ownership, and develop versatile skills.
📈 Long-Term Career Path
With the right dedication, you can grow into roles such as:
- Clinical SAS Programmer
- Statistical Programmer
- Lead Programmer
- Data Standards Specialist
🏢 Why Hyderabad is a Great Career Hub
Hyderabad has become one of India’s leading pharmaceutical and biotech centers. With multiple global pharma companies and CROs operating here, the city offers abundant opportunities in:
- Clinical research
- Data management
- Regulatory affairs
- Pharmacovigilance
- Biostatistics
Starting your career in Hyderabad means being surrounded by a strong professional ecosystem and networking opportunities. 🌆
📝 How to Apply?
Interested candidates can:
📧 Send their resume to: HR@panakeia.in
🌐 Apply through the official Panakeia Careers page
Make sure your resume highlights:
- Educational qualifications
- SAS/R certifications (if any)
- Academic projects related to statistics or clinical data
- Internship or training experience
- Knowledge of CDISC standards
Pro Tip: Customize your resume to align with SDTM, ADaM, and TFL keywords for better visibility. 🎯
🔎 Who Should Definitely Apply?
✅ Freshers from Life Sciences, Statistics, Mathematics, Biotechnology
✅ Candidates trained in Clinical SAS
✅ Professionals with 0–2 years of relevant experience
✅ Self-learners who enjoy analytical thinking
✅ Individuals serious about building a career in Clinical Research
If you are ready to build a strong foundation in Clinical Programming, this is your moment! 💪
📌 Final Thoughts
Breaking into the pharmaceutical or CRO industry can feel overwhelming—but opportunities like this make it easier. With structured mentorship, real-world exposure, and a strong learning environment, you can build a stable and rewarding career in Clinical SAS & R.
The demand for skilled clinical programmers continues to grow, especially those who understand CDISC standards, dataset validation, and statistical reporting.
If you’re ambitious, detail-oriented, and eager to grow in the pharma industry, don’t wait. Take the next step in your Clinical SAS journey today! 🚀✨
