Parexel Data Surveillance Analyst Jobs Remote
Exciting Parexel Data Surveillance Analyst Jobs 2026 | Remote Clinical Data Careers
Parexel is hiring for the position of Data Surveillance Analyst (DSA) in India. This fully remote opportunity is ideal for professionals with experience in clinical research, data management, centralized monitoring, risk-based quality management (RBQM), and clinical data analytics.
Candidates with backgrounds in Life Sciences, Pharmacy, Clinical Research, Data Management, Biostatistics, or Data Analytics can explore this exciting career opportunity with one of the world’s leading Clinical Research Organizations (CROs).
About Parexel
Parexel is a global clinical research organization that helps pharmaceutical, biotechnology, and medical device companies develop innovative therapies. The company supports clinical trials worldwide through expertise in regulatory affairs, clinical operations, data management, biostatistics, pharmacovigilance, and technology-driven research solutions.
Position Details
Job Title: Data Surveillance Analyst
Job ID: R0000042355
Location: Remote, India
Category: Clinical Trials
Work Model: Fully Remote
Company: Parexel
Key Responsibilities
The Data Surveillance Analyst will support centralized monitoring activities, data quality reviews, risk identification, and project-level surveillance activities.
Data Surveillance Planning
- Support the development of Data Surveillance Plans (DSPs).
- Assist in defining Key Risk Indicators (KRIs).
- Configure Quality Tolerance Limits (QTLs).
- Support central statistical monitoring activities.
- Configure and maintain CluePoints Central Monitoring Platform.
Data Review and Analysis
- Review study data using centralized monitoring technologies.
- Identify data trends, outliers, and potential quality issues.
- Analyze project-specific Quality Tolerance Limits.
- Perform periodic surveillance reviews according to the Data Surveillance Plan.
- Document findings and recommendations.
Technology & System Management
- Configure data imports and mappings.
- Set up standard and customized KRIs.
- Maintain statistical analysis parameters.
- Support issue tracking and resolution activities.
Risk Management & Monitoring
- Detect emerging risks and data quality signals.
- Escalate critical issues to project leadership.
- Support adaptive monitoring and risk-based monitoring activities.
- Participate in review meetings and decision-making processes.
Reporting & Documentation
- Prepare Central Monitoring Reports.
- Maintain issue management documentation.
- Support client-ready presentations and reports.
- Collaborate with Data Surveillance team members to consolidate findings.
Eligibility Criteria
Educational Qualification
Candidates should possess:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Biostatistics
- Data Analytics
- Biological Sciences
- Clinical Research
- Or equivalent relevant degree
Experience Required
- Minimum 2 years of relevant experience in:
- Clinical Research
- Clinical Data Management
- Centralized Monitoring
- Risk-Based Monitoring (RBM)
- Data Surveillance
- Medical Data Review
Required Skills
Clinical Research Skills
- Risk-Based Quality Management (RBQM)
- Centralized Monitoring
- Data Surveillance Processes
- Clinical Trial Operations
- ICH-GCP Guidelines
- Clinical Data Review
Data Analytics Skills
- Data Trend Analysis
- Signal Detection
- Data Quality Assessment
- Risk Identification
- Statistical Monitoring
Technical Skills
- Basic SAS Programming
- SQL Scripting
- CluePoints Platform
- CTMS
- EDMS
- Microsoft Office Suite
Additional Skills
- Strong analytical thinking
- Problem-solving abilities
- Attention to detail
- Presentation skills
- Stakeholder communication
- Cross-functional collaboration
Preferred Experience
Candidates with experience in the following areas will have an advantage:
- Adaptive Monitoring Design Studies
- Central Monitoring Programs
- Risk-Based Monitoring Studies
- Data Surveillance Operations
- Clinical Data Management
- Statistical Monitoring Activities
- Regulatory Inspection Support
How to Apply
Interested candidates can apply through the official Parexel careers portal:
https://jobs.parexel.com/en/job/-/-/877/96294689008
Applicants should highlight experience in centralized monitoring, clinical data review, SAS programming, SQL, RBQM processes, and data surveillance activities in their resumes.
Frequently Asked Questions (FAQs)
1. Is this a remote position?
Yes. This is a fully remote opportunity based in India.
2. What qualifications are eligible?
Life Sciences, Pharmacy, Clinical Research, Biological Sciences, Data Analytics, and related disciplines.
3. Is SAS knowledge required?
Yes. Basic SAS programming skills are required. SQL scripting knowledge is also beneficial.
4. How much experience is needed?
A minimum of 2 years of relevant experience in clinical research, data management, or monitoring is recommended.
5. What is the primary focus of this role?
The role focuses on centralized monitoring, risk-based quality management, data surveillance, trend analysis, and clinical data quality oversight.
6. Which technologies are used?
CluePoints, CTMS, EDMS, SAS, SQL, and various clinical trial management platforms.
Job Overview
| Category | Details |
|---|---|
| Company | Parexel |
| Position | Data Surveillance Analyst |
| Qualification | B.Pharm, M.Pharm, Pharm.D, Life Sciences |
| Experience | 2+ Years |
| Location | Remote, India |
| Department | Clinical Trials |
| Work Mode | Fully Remote |
| Skills | RBQM, SAS, SQL, Central Monitoring |
To apply for this job please visit jobs.parexel.com.
