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Job Overview
Location
India
Job Type
Full-time
Category
Data Science
Date Posted
November 2, 2025
Full Job Description
đź“‹ Description
- • Join Medable as a Data Scientist and become the analytical engine behind life-changing clinical trials. You will design, build, and deploy algorithms that turn raw trial data into clear, actionable insights, directly accelerating the delivery of new therapies to patients who need them most.
- • Own the end-to-end data pipeline for assigned studies: ingest multi-modal data from EDC, eCOA, ePRO, labs, imaging, and wearable devices; cleanse, transform, and validate data to ensure regulatory-grade quality; and automate recurring data transfers so that stakeholders receive fresh, reliable information every day.
- • Develop statistical models and machine-learning solutions that predict patient enrollment, identify protocol deviations, flag safety signals, and optimize site performance. Your work will be embedded in our cloud platform and surfaced through interactive dashboards that clinicians, monitors, and executives rely on for real-time decision-making.
- • Craft visually compelling narratives with R Shiny, Looker, and SpotFire that translate complex statistical findings into intuitive graphics. Whether you are presenting to a cross-functional internal squad or to external sponsors and regulators, your storytelling will make data approachable and drive faster consensus.
- • Represent the Data Science function in sprint planning, design reviews, and client workshops. You will translate business questions into analytical requirements, scope feasibility, and negotiate timelines—ensuring that every analysis we ship creates measurable value for patients and partners.
- • Champion continuous improvement by documenting best practices, contributing to our internal R and Python packages, and mentoring junior analysts. Under the guidance of Senior Data Scientists, you will pilot new methodologies (e.g., Bayesian adaptive designs, synthetic control arms) that keep Medable at the cutting edge of digital trials.
- • Collaborate tightly with Product, Engineering, Regulatory, and Clinical Operations to ensure that every algorithm meets GCP, 21 CFR Part 11, and GDPR standards. You will participate in validation testing, author technical specifications, and support audit inquiries with clear, traceable documentation.
- • Monitor the performance of deployed models in production, set up automated alerts for data drift or anomalies, and iterate rapidly based on user feedback. Your proactive maintenance will safeguard trial integrity and uphold our reputation for delivering trustworthy evidence.
- • Contribute to strategic R&D initiatives such as digital biomarker discovery, patient-centric trial design, and decentralized trial analytics. Your curiosity and creativity will help Medable unlock new scientific insights and expand the boundaries of what is possible in clinical research.
- • Embrace a culture of bold experimentation, transparent communication, and relentless focus on patient impact. At Medable, your code, analyses, and recommendations will ripple through the entire drug-development ecosystem, shortening the path from bench to bedside.
🎯 Requirements
- • 2+ years of hands-on experience in data science, statistics, or programming roles within healthcare, life sciences, or a regulated industry
- • Bachelor’s degree in Mathematics, Statistics, Data Science, Computer Science, or related quantitative discipline
- • Advanced proficiency in R and Python for data manipulation, statistical modeling, and visualization; working knowledge of SQL and SAS for clinical datasets
- • Demonstrated ability to translate complex analytical results into clear, business-oriented narratives for both technical and non-technical stakeholders
- • Experience with cloud platforms (AWS, GCP, or Azure), version control (Git), and reproducible research practices; familiarity with clinical data standards (CDISC, SDTM, ADaM) is a strong plus
🏖️ Benefits
- • Hybrid work model from day one—split your time between home and our modern offices in Bangalore or Pune, with flexible hours that fit your life
- • Competitive compensation package including annual performance bonuses and employee stock options, aligning your success with Medable’s rapid growth
- • Comprehensive health insurance for you and your dependents, plus inclusive parental leave for non-birthing parents and generous PTO
- • Dedicated volunteer time off and peer-to-peer recognition programs that celebrate your impact on patients, colleagues, and communities
Skills & Technologies
About Medable Inc.
Medable provides a cloud-based platform that enables pharmaceutical companies, biotech firms and academic centers to design, conduct and manage decentralized and hybrid clinical trials. The software integrates electronic consent, telehealth, remote data capture, wearables and ePRO into one compliant environment, reducing site burden and accelerating patient recruitment across global populations. Built with regulatory-grade security and privacy controls, the platform supports real-time analytics and adaptive study designs while maintaining FDA, EMA and PMDA compliance. Medable's technology is used in hundreds of trials spanning oncology, rare disease, neuroscience and cardiovascular therapeutic areas, delivering faster insights and more diverse patient participation.
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