Apply for Data Surveillance Analyst Parexel job 2026. Check eligibility, remote role, skills required, and application process for clinical research professionals.
Introduction
If you are interested in clinical data analysis, risk-based monitoring, and clinical trial quality management, this opportunity can be a strong career move. Parexel is hiring Data Surveillance Analysts to support global clinical trials through advanced data monitoring and analytics. This remote role is ideal for candidates with experience in clinical research, data management, or analytics who want to work on cutting-edge projects in the pharmaceutical industry.
Job Overview
| Particulars | Details |
|---|---|
| Job Title | Data Surveillance Analyst |
| Company Name | Parexel |
| Location | Remote (India) |
| Employment Type | Full-Time |
| Department | Clinical Trials / Data Surveillance |
| Experience Required | 2+ Years |
| Education | Life Sciences / Pharmacy / Data Analytics |
| Salary | As per company norms |
Company Overview
Parexel is a leading global Clinical Research Organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies in drug development. The company is known for delivering high-quality clinical trial solutions, regulatory consulting, and data-driven insights to improve patient outcomes worldwide.
Job Location & Employment Type
This is a fully remote opportunity based in India, allowing professionals to work from home while collaborating with global clinical teams. The position is full-time and offers long-term growth in clinical data science and monitoring.
Open Positions / Department Details
The Data Surveillance Analyst role is part of Parexel’s Clinical Trials and Risk-Based Quality Management (RBQM) team. The department focuses on centralized monitoring, data surveillance, and ensuring data integrity in clinical studies.
Key Roles & Responsibilities
Data Surveillance Plan Development
- Assist in creating Data Surveillance Plans (DSPs) with Key Risk Indicators (KRIs)
- Define Quality Tolerance Limits (QTLs) and statistical analysis parameters
- Configure and maintain surveillance tools like CluePoints platform
- Set up data mapping for multiple clinical data sources
Data Monitoring & Review
- Analyze clinical trial data to identify trends, risks, and inconsistencies
- Perform centralized monitoring activities as per project requirements
- Document findings in tracking systems and reports
- Identify outliers and data quality issues for further investigation
Collaboration & Communication
- Participate in internal and external project meetings
- Present data findings and insights to stakeholders
- Collaborate with cross-functional teams for issue resolution
- Support audit and regulatory inspection processes
Risk Identification & Issue Management
- Detect signals related to study non-compliance or delays
- Escalate critical issues to appropriate teams
- Support decision-making with data-driven insights
- Track and manage issues through monitoring systems
Reporting & Documentation
- Prepare Central Monitoring Reports
- Maintain documentation in compliance with regulatory standards
- Ensure timely submission of reports and updates
- Support continuous improvement initiatives
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medical Sciences, or Data Analytics
- Equivalent qualifications in clinical or technology-related fields are also acceptable
Experience
- Minimum 2 years of experience in clinical research, data management, or medical field
- Experience in centralized monitoring or RBQM processes is preferred
Skills Required
- Knowledge of clinical trial processes and ICH-GCP guidelines
- Understanding of centralized monitoring and data surveillance methods
- Basic SAS programming or SQL knowledge
- Strong data analysis and problem-solving skills
- Familiarity with CTMS, EDMS, and MS Office tools
- Excellent communication and presentation skills
- Ability to work in global and cross-functional teams
- Strong time management and multitasking ability
Salary & Benefits
- Salary: As per company norms
- Work-from-home flexibility
- Exposure to global clinical trial projects
- Opportunity to develop skills in data analytics and RBQM
- Career growth in clinical data science and monitoring
Selection Process
The typical hiring process includes:
- Resume screening
- HR interview
- Technical interview (data analysis / clinical concepts)
- Final interview
How to Apply
Interested candidates can apply online through the official Parexel careers portal. Make sure your resume highlights experience in clinical trials, data analysis, or centralized monitoring.
Important Dates
- Application Deadline: Not specified (Apply as soon as possible)
Why Apply for This Job?
This Data Surveillance Analyst at Parexel 2026 role is a great opportunity for professionals aiming to build a career in clinical data analytics and risk-based monitoring. With increasing demand for data-driven decision-making in clinical trials, this role offers strong future growth potential.
Working with Parexel allows you to collaborate with global experts, gain hands-on experience with advanced monitoring tools, and develop expertise in regulatory-compliant data analysis. The remote setup also provides flexibility and work-life balance, making it an attractive option for professionals across India.
FAQs
1. What is the focus keyword for this job?
The focus keyword is “Data Surveillance Analyst Parexel”.
2. Is this job remote?
Yes, this is a fully remote role based in India.
3. What experience is required?
A minimum of 2 years of relevant experience in clinical research or data management is recommended.
4. What technical skills are needed?
Basic SAS or SQL knowledge, data analysis skills, and familiarity with clinical trial systems are required.
5. How can I apply for this job?
You can apply online through Parexel’s official careers website.
Conclusion
The Data Surveillance Analyst at Parexel offers a valuable opportunity for professionals interested in clinical data analysis and centralized monitoring. With strong career growth, global exposure, and remote flexibility, this role is ideal for candidates looking to advance in the pharmaceutical and clinical research industry. Apply soon to secure your chance.
Disclaimer
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