Parexel is hiring for the position of Data Surveillance Analyst (DSA) under its Clinical Trials category. The role is listed for India – Remote and is suitable for professionals with experience in medical, clinical, data management, or related areas.
The Data Surveillance Analyst will work with scientific and operational data to support Data Surveillance Plans, Quality Tolerance Limits, risk indicators, statistical analysis, and central monitoring activities. The position also involves identifying data quality trends, unusual findings, and emerging issues and communicating relevant findings to project teams.
Candidates with a relevant degree, 2 or more years of relevant experience, and knowledge of SAS programming and/or SQL may be considered for this opportunity.
Parexel Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Parexel |
| Job Title | Data Surveillance Analyst |
| Job Requisition ID | R0000045688 |
| Category | Clinical Trials |
| Job Location | India – Remote |
| Employment Type | Not specified in the provided details |
| Experience | 2+ years of relevant experience recommended |
| Education | Degree in Medical, Biological Science, Pharmacy, Data Analytics or related field |
| Key Skills | Data Analysis, SAS, SQL, Central Monitoring, RBQM |
| Work Mode | Remote |
| Salary / CTC | Not specified |
| Application Mode | Online |
About Parexel
Parexel is a global clinical research and healthcare services organization supporting clinical development and related activities.
The Data Surveillance Analyst role is focused on analyzing clinical and operational information to support risk-based quality management and data surveillance activities during clinical studies.
Job Description
The Data Surveillance Analyst is responsible for analyzing scientific and operational data in accordance with project-specific Data Surveillance Plans. The role includes reviewing Quality Tolerance Limits (QTLs), supporting surveillance plan development, configuring relevant surveillance technologies, and performing defined reviews.
The analyst will also participate in internal and external meetings when required and communicate significant findings, trends, risk indicators, and potential data-quality concerns to appropriate project stakeholders.
Data Surveillance Analyst
The position combines clinical data analysis, central monitoring, statistical review, technology configuration, risk identification, and issue management. The selected candidate will work with project teams and technology stakeholders to identify potential data-quality concerns and support appropriate follow-up actions.
Educational Qualification
Candidates should have a degree-level qualification. Preferred educational backgrounds include:
- Medical sciences
- Biological sciences
- Pharmacy
- Data analytics
- Related clinical disciplines
- Relevant technology or business qualifications may also be considered as equivalent backgrounds
The role requires an educational background relevant to clinical, scientific, technology, or data-related work.
Experience Requirements
The vacancy recommends 2 or more years of relevant experience in areas such as:
- Medical work
- Clinical research
- Clinical data management
- Data-related functions
Experience with an adaptive monitoring design study or participation in a Central Monitoring/Data Surveillance process is highly recommended.
Candidates should also have:
- Basic SAS programming skills
- SAS programming and/or SQL script-writing experience
- Understanding of clinical data operations
Required Technical Skills
Data Analysis
Candidates should be proficient in:
- Data analysis
- Trend identification
- Identification of unusual or atypical data
- Issue triage
- Data-quality assessment
- Interpretation of risk indicators and quality signals
SAS and SQL
The position requires basic SAS programming and/or SQL script-writing skills.
These skills are relevant for analyzing clinical and operational datasets and supporting surveillance activities.
Clinical Data Knowledge
A basic understanding of:
- SDTM domains
- Clinical data operations
- Data surveillance processes
- Central monitoring
- Data-driven monitoring
- Risk-based quality management
is expected.
Relevant Systems
The role mentions proficiency with relevant software and technologies, including:
- CTMS
- EDMS
- Microsoft Office
- Parexel-specific surveillance technologies
- Central monitoring platforms such as Clue Points
Key Responsibilities
1. Data Surveillance Plan Development
The selected candidate will support the development and implementation of project-specific Data Surveillance Plans.
Responsibilities may include:
- Supporting the definition of Key Risk Indicators (KRIs).
- Supporting Quality Tolerance Limit development.
- Assisting with central statistical analysis requirements.
- Setting up statistical analysis parameters.
- Creating data-import mappings for different data sources.
- Supporting the configuration of standard and project-specific KRIs.
2. Data Surveillance Technology Configuration
The role involves configuring and maintaining technologies used for data surveillance.
This may include:
- Maintaining surveillance technology configurations.
- Refreshing technology settings for each review cycle according to the Data Surveillance Plan.
- Creating and configuring standard and customized KRIs.
- Supporting statistical analysis configurations.
- Working with technology teams to identify suitable solutions.
3. Data Surveillance Reviews
The analyst will review relevant scientific and operational information according to the project-specific surveillance plan.
Activities may include:
- Performing assigned data surveillance reviews.
- Reviewing data from defined technology platforms and other relevant sources.
- Identifying data-quality trends and outliers.
- Detecting emerging issues and quality signals.
- Performing core reviews according to the Data Surveillance Plan.
- Documenting atypical data findings.
- Correlating findings from multiple data sources.
4. Findings and Issue Management
The selected candidate will document surveillance findings and support appropriate issue management.
This may involve:
- Recording findings in the Data Findings Form.
- Updating issue tracking systems.
- Supporting documentation of actions in the Clue Points Issue Management system.
- Identifying potential follow-up requirements.
- Escalating significant study or site issues to the appropriate Functional Lead when immediate action is required.
5. Project Meetings and Collaboration
The position requires collaboration with project teams and other stakeholders.
Responsibilities include:
- Participating in Data Surveillance meetings.
- Supporting Data Surveillance review meetings.
- Helping drive reviews and decisions when required.
- Working with team members to agree on appropriate actions.
- Compiling signals and actions into client-ready information.
- Participating in investigator meetings when required.
- Supporting internal and external meetings and audits or regulatory inspections as applicable.
6. Central Monitoring Reporting
The role also includes:
- Supporting preparation of Central Monitoring Reports.
- Completing, sharing, and filing required reports.
- Maintaining appropriate documentation of surveillance activities.
- Supporting follow-up actions arising from surveillance findings.
Risk-Based Quality Management
The role requires knowledge of Risk-Based Quality Management (RBQM) processes and data surveillance methods.
Candidates should understand how clinical study data can be reviewed to identify:
- Risk indicators
- Quality signals
- Data trends
- Outliers
- Potential study issues
- Site-level concerns
- Data-quality problems
- Emerging issues requiring follow-up
Experience with centralized or data-driven monitoring is particularly relevant to this position.
Compliance and Regulatory Requirements
The selected candidate will be expected to maintain working knowledge of and comply with applicable:
- ICH-GCP guidelines
- International regulations
- Local regulatory requirements
- Parexel SOPs
- Parexel training requirements
- Sponsor-specific training requirements
- Study-specific procedures
The role also requires appropriate escalation of significant compliance, quality, site, or study issues.
Communication and Teamwork Skills
Because the position operates within global and virtual teams, candidates should have:
- Strong interpersonal skills
- Excellent verbal and written communication
- Presentation skills
- Client-focused approach
- Strong quality orientation
- Ability to work in matrix environments
- Ability to collaborate with global virtual teams
- Strong time management
- Multitasking ability
- Ability to work independently with limited supervision
Work Location and Work Mode
Location: India – Remote
The vacancy is listed as a remote position. The provided job information does not specify fixed working hours or shift timings.
Candidates should confirm any role-specific working-hour requirements during the recruitment process.
Salary / CTC
The salary or CTC for the Parexel Data Surveillance Analyst position has not been specified in the provided vacancy details.
Candidates should confirm compensation and employment terms directly through the official recruitment process.
Selection Process
A detailed selection process has not been specified in the provided job description.
Depending on the recruitment process, candidates may be assessed on their relevant clinical/data management experience, data analysis capabilities, SAS or SQL knowledge, communication skills, and understanding of clinical data surveillance concepts.
How to Apply for Parexel Recruitment 2026
Interested and eligible candidates can submit their application online through the official Parexel careers portal.
Candidates should review the complete job description and provide accurate information about their education, professional experience, technical skills, and clinical research background.
Important Details Before Applying
- The position is for Data Surveillance Analyst.
- Job ID is R0000045688.
- The listed location is India – Remote.
- The role falls under the Clinical Trials category.
- A degree-level qualification is required.
- Medical, biological science, pharmacy, and data analytics backgrounds are preferred.
- 2+ years of relevant medical, clinical, or data management experience is recommended.
- Basic SAS programming and/or SQL script writing is required.
- Knowledge of centralized monitoring and data-driven monitoring is relevant.
- Experience with adaptive monitoring or Data Surveillance processes is highly recommended.
- Salary information is not disclosed in the provided vacancy.
- Candidates should verify the latest job status and requirements before applying.
Frequently Asked Questions
1. What is the job title at Parexel?
The position is Data Surveillance Analyst.
2. What is the Parexel job requisition ID?
The job requisition ID is R0000045688.
3. Where is the Data Surveillance Analyst job located?
The position is listed as India – Remote.
4. What educational qualification is required?
A degree-level qualification is expected. Medical, biological science, pharmacy, and data analytics backgrounds are preferred.
5. How much experience is required?
The vacancy recommends 2 or more years of relevant medical, clinical, or data management experience.
6. Is SAS knowledge required?
Yes. The vacancy specifies basic SAS programming skills and mentions SAS programming and/or SQL script writing as a requirement.
7. Is SQL knowledge required?
Basic SQL script-writing knowledge is mentioned as part of the technical requirements.
8. What is Data Surveillance?
In this role, Data Surveillance involves analyzing scientific and operational data to identify trends, risk indicators, outliers, quality signals, and potential issues according to a project-specific Data Surveillance Plan.
9. What systems are mentioned for this role?
The vacancy mentions CTMS, EDMS, Microsoft Office, Parexel-specific technologies, and platforms such as Clue Points Central Monitoring Platform.
10. Is the salary mentioned?
No. The salary/CTC is not specified in the provided vacancy information.
Important Note
Job requirements, vacancy status, recruitment timelines, compensation, and employment conditions may change. Candidates should verify the latest information on the official Parexel careers portal before applying. Application submission does not guarantee selection or employment.