Data Surveillance Analyst Remote Job at Parexel role in Bengaluru. Apply before March 31, 2026 for clinical data and RBQM job opportunity.
Professionals with experience in clinical data, analytics, and monitoring now have an exciting opportunity to work with a global CRO. Parexel is hiring Data Surveillance Analysts to support risk-based monitoring and centralized data review processes. This role is ideal for candidates with clinical research or data management experience who want to grow in data-driven clinical operations.
Company Overview
Parexel is a leading Contract Research Organization (CRO) providing clinical development, regulatory, and consulting services to pharmaceutical and biotechnology companies worldwide. With a strong focus on improving patient outcomes, Parexel is known for its expertise in clinical trials, data analytics, and regulatory excellence.
Job Overview (Job Details)
| Category | Details |
|---|---|
| Organization | Parexel |
| Role | Data Surveillance Analyst |
| Qualification | Degree in Life Sciences / Pharmacy / Data Analytics |
| Experience | 2+ Years |
| Job Location | Remote (India – Bengaluru base) |
| Employment Type | Full-Time |
| Application Mode | Online |
| Salary | Not Disclosed |
Job Location & Employment Type
This is a remote role based in Bengaluru, offering flexibility while working on global clinical projects. It is a full-time position within the clinical data and monitoring function.
Open Positions / Department Details
The hiring is for the Data Surveillance / Risk-Based Quality Management (RBQM) team. The role focuses on centralized monitoring, data review, and identifying trends or risks in clinical trial data.
Key Roles & Responsibilities
Candidates selected for this role will be responsible for:
Data Surveillance Plan & Setup
- Supporting development of Data Surveillance Plans (DSPs)
- Configuring monitoring tools like CluePoints platform
- Setting up Key Risk Indicators (KRIs) and Quality Tolerance Limits
Data Review & Monitoring
- Reviewing clinical and operational data for trends and anomalies
- Identifying data quality issues, outliers, and compliance risks
- Documenting findings and maintaining issue tracking systems
- Performing central monitoring reviews as per study plans
Reporting & Collaboration
- Presenting findings in internal and external meetings
- Supporting audit readiness and regulatory inspections
- Collaborating with cross-functional teams and technology groups
- Preparing central monitoring and surveillance reports
Compliance & Quality
- Ensuring adherence to ICH-GCP and regulatory standards
- Supporting risk-based monitoring and data-driven decision-making
- Maintaining documentation and compliance with SOPs
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences, Pharmacy, Medical, or Data Analytics
- Equivalent clinical or technical qualification may also be considered
Experience
- Minimum 2+ years in clinical research, data management, or analytics
- Experience in centralized monitoring or data surveillance preferred
Skills Required
- Knowledge of RBQM (Risk-Based Quality Management) processes
- Understanding of centralized monitoring and clinical data review
- Basic SAS programming and/or SQL skills
- Familiarity with SDTM domains and clinical data standards
- Proficiency in tools like CTMS, EDMS, and MS Office
- Strong analytical and problem-solving skills
- Excellent communication and teamwork abilities
Salary & Benefits
- Salary: Not disclosed
- Remote working flexibility
- Opportunity to work on global clinical trials
- Exposure to advanced data monitoring technologies
- Career growth in clinical data analytics and RBQM
- Collaborative and international work environment
Selection Process
The hiring process typically includes:
- Online Application
- Resume Screening
- Technical Interview (Data Analysis & Clinical Concepts)
- HR Discussion
- Final Selection
How to Apply
Interested candidates can apply through the official Parexel careers portal before the deadline.
Important Dates
- Application Deadline: March 31, 2026
Why Apply for This Pharma Job?
This role is perfect for professionals looking to transition into data-driven clinical research. Data Surveillance Analysts play a key role in improving trial quality, identifying risks early, and ensuring regulatory compliance.
With the increasing adoption of centralized monitoring and AI-driven analytics in clinical trials, this role offers strong future growth and global career opportunities in clinical data science.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with any company or recruiter. We do not charge any fee for job applications. Candidates should verify all details independently before applying.
Final Call-to-Action
If you have experience in clinical data, analytics, or monitoring, this is a great opportunity to work with a global CRO. Apply now and take your career forward in clinical data surveillance.
