Clinical Data Management Analyst

Why This Role Matters
Clinical trials generate large volumes of complex data that must be captured, validated, and analyzed accurately to ensure the safety and effectiveness of medicines and vaccines. The Analyst role within Data Science & Management functions at GSK plays a key role in managing clinical trial data systems and ensuring high data quality throughout the research lifecycle.
This role supports the development and maintenance of electronic data capture systems, manages patient-reported outcomes platforms, and ensures that clinical trial data meets regulatory standards. By supporting accurate data collection and analysis, professionals in this role contribute directly to the development of innovative treatments and vaccines that improve global health outcomes.

Job Description
The Analyst in Data Science & Management sub-functions will support the technical development and management of clinical data systems used in research studies. The role focuses on electronic data capture (eDC), electronic patient-reported outcomes (ePRO), and vendor data integration.
The analyst will assist in system configuration, automation initiatives, and clinical data validation processes while ensuring compliance with regulatory standards and company procedures.
This role also involves collaboration with IT teams, clinical systems specialists, and external vendors to ensure smooth data flow and system functionality during clinical trials. Strong attention to detail, analytical thinking, and adherence to documentation standards are essential for success in this position.

Key Features of the Role:
• Opportunity to work in clinical data management within a global pharmaceutical organization
• Exposure to clinical trial technologies such as eDC and ePRO systems
• Hands-on experience in clinical data validation, analysis, and regulatory documentation
• Collaboration with clinical research teams, IT specialists, and external vendors
• Opportunity to contribute to automation and process improvements in clinical operations
• Career development in clinical data management, clinical research, and data science

Responsibilities
• Support the technical development of electronic Data Capture (eDC) systems used in clinical trials
• Assist in the implementation and management of electronic Patient-Reported Outcomes (ePRO) platforms
• Facilitate technical acquisition and integration of vendor-provided clinical data
• Participate in automation initiatives and assist in the development or maintenance of internal tools
• Apply technical expertise in areas such as programming, user acceptance testing (UAT), data validation, and clinical data analysis
• Support data cleaning and validation activities to ensure accuracy and completeness of clinical trial data
• Assist in the preparation of data and documentation required for regulatory submissions
• Contribute to the creation and maintenance of quality plans at the clinical study level
• Ensure that all task-related documentation is accurately stored within the electronic Trial Master File (eTMF) system
• Follow departmental standard operating procedures, corporate policies, and regulatory requirements
• Complete all required training programs through company learning platforms
• Prepare reports, provide updates, and communicate observations related to daily tasks and processes
• Participate in after-action reviews to identify lessons learned and process improvements
• Collaborate with IT teams, clinical systems teams, and external vendors supporting study applications

Required Qualifications

Educational Requirements:
• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or related biomedical fields
• Degrees such as B.Pharm, M.Pharm, Pharm.D, BSc, or MSc in Life Sciences are commonly considered relevant
• Additional certification or training in clinical research or data management may be advantageous

Experience and Skills:
• Understanding of clinical trial processes and clinical data management principles
• Familiarity with electronic Data Capture (eDC) systems used in clinical trials
• Knowledge of electronic Patient-Reported Outcomes (ePRO) platforms
• Basic understanding of programming, system validation, or user acceptance testing
• Experience in clinical data cleaning, analysis, and validation processes
• Strong analytical and problem-solving skills
• Ability to manage documentation accurately in systems like eTMF
• Knowledge of regulatory requirements and industry best practices for clinical trials
• Strong communication and collaboration skills for working with cross-functional teams
• Ability to identify process improvement opportunities and support automation initiatives
• Good organizational and time-management skills

Salary Insights:
• Entry-level Clinical Data Analysts typically earn ₹4 LPA – ₹8 LPA in India
• Professionals with relevant clinical data management experience may earn ₹8 LPA – ₹12 LPA depending on skills and experience
• Additional benefits may include health insurance, performance bonuses, and professional training opportunities

Company Overview
GSK (GlaxoSmithKline) is a leading global biopharmaceutical company focused on improving human health through scientific innovation. The company works to prevent and treat diseases by developing specialty medicines and vaccines across multiple therapeutic areas including respiratory diseases, immunology, oncology, HIV, and infectious diseases.
With a mission to unite science, technology, and talent to get ahead of disease together, GSK aims to positively impact the health of billions of people worldwide. The organization supports scientific research, patient care, and public health initiatives while maintaining strong commitments to ethics, compliance, and diversity in the workplace.

FAQs

What does a Clinical Data Management Analyst do?
A Clinical Data Management Analyst manages clinical trial data systems, validates research data, and ensures accuracy and compliance during drug development studies.

What are eDC and ePRO systems?
Electronic Data Capture (eDC) systems collect clinical trial data digitally, while electronic Patient-Reported Outcomes (ePRO) systems gather health information directly from patients participating in studies.

Is prior clinical research experience required?
While not always mandatory, experience in clinical data management, clinical trials, or healthcare data analysis can be beneficial.

What skills are important for this role?
Key skills include data analysis, system validation, documentation management, regulatory compliance knowledge, and strong attention to detail.

Application Tips
• Highlight experience in clinical research, data management, or healthcare analytics
• Mention familiarity with eDC systems, ePRO tools, or clinical databases
• Emphasize analytical, documentation, and data validation skills
• Demonstrate understanding of regulatory compliance and clinical research standards
• Include examples of projects or training related to clinical data management or healthcare technology.