Location: Mumbai, Maharashtra, India (Remote)
Job Type: Full-Time
Job ID: R63408
Company: Medtronic
Experience Required:
0–2 years (Eligible for freshers with advanced degree)
2+ years (Bachelor’s degree candidates)
About the Company
Medtronic is a global leader in healthcare technology, focused on improving patient outcomes through innovation, research, and advanced medical solutions. With a strong mission to alleviate pain, restore health, and extend life, Medtronic operates across multiple therapeutic areas, impacting millions of lives worldwide.
Job Overview
This role is ideal for professionals looking to build or advance their career in clinical SAS programming and biostatistics within clinical research. As part of the Biostats and Clinical Intelligence (BCI) team under Medtronic Clinical & Regulatory Solutions (MCRS), you will contribute to statistical programming, clinical data analysis, and regulatory submissions for complex studies including PMA (Premarket Approval) trials.
Key Responsibilities
Design, develop, and validate SAS programs for clinical data analysis
Perform statistical programming for complex clinical studies and regulatory submissions
Identify data inconsistencies and support data cleaning and resolution processes
Develop and maintain analysis datasets including ADaM and SDTM structures
Review Statistical Analysis Plans (SAP) from a programming perspective
Support integration of data from multiple studies and sources
Program, test, document, and validate statistical outputs in compliance with industry standards
Collaborate with cross-functional teams including Biostatistics, Data Management, and Clinical Operations
Participate in client interactions, project planning, and timeline management
Assist in SOP development, training material creation, and process improvements
Mentor junior programmers and coordinate with vendors or outsourcing partners when required
Minimum Qualifications (Must Have)
Bachelor’s degree with minimum 2 years of SAS programming or data analysis experience
OR
Master’s/Advanced degree (freshers eligible)
Certification in SAS Base Programming (Mandatory)
Preferred Qualifications (Nice to Have)
Master’s degree in Computer Science, Statistics, or related field
3–5 years of SAS programming experience in clinical research
Hands-on experience with ADaM and SDTM datasets
Knowledge of PL/SQL, Unix scripting, Python, or R
Experience in statistical programming for clinical trials
Exposure to pharmaceutical, biotech, or medical device industry
Understanding of clinical trial lifecycle and regulatory requirements
Key Skills & Competencies
Strong analytical and problem-solving skills
Expertise in SAS programming for clinical data
Knowledge of ICH-GCP and clinical research standards
Effective communication and stakeholder management
Ability to manage timelines and deliverables in a fast-paced environment
Work Environment & Growth Opportunities
Opportunity to work on global clinical trials and regulatory projects
Exposure to advanced statistical programming and clinical data systems
Collaborative and innovation-driven culture
Strong career growth in clinical SAS programming and biostatistics
Compensation & Benefits
Competitive salary package
Performance-based incentives (Medtronic Incentive Plan – MIP)
Comprehensive employee benefits and wellness programs
Career development and learning opportunities
About the Team (MCRS)
Medtronic Clinical & Regulatory Solutions (MCRS) provides end-to-end clinical research services including:
Clinical Operations and Monitoring
Data Management and Clinical Safety
Evidence Generation and Scientific Solutions
Operational Excellence and Analytics
Important Note for Applicants
This role is open to both freshers (with advanced degrees) and experienced professionals (2+ years) in SAS programming or clinical data analysis. Candidates with strong technical expertise and interest in clinical research are highly encouraged to apply.
How to Apply
Apply directly through the company careers portal or explore similar global opportunities on ThePharmaDaily.com – your trusted platform for verified pharma, clinical research, and pharmacovigilance jobs.
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