Apply for Parexel Data Surveillance Analyst remote job in India. Check eligibility, clinical data monitoring responsibilities, skills, and application process.
Introduction
Candidates interested in clinical data analytics, risk-based monitoring, and central data review now have an excellent opportunity to work with a leading CRO. This role focuses on analyzing clinical trial data, identifying trends, and ensuring study quality through advanced surveillance techniques. It is ideal for professionals looking to grow in clinical data science and centralized monitoring.
Company Overview
Parexel is a globally renowned Contract Research Organization (CRO) offering clinical development, regulatory consulting, and data-driven solutions to pharmaceutical and biotechnology companies. With a strong emphasis on innovation and quality, Parexel supports global clinical trials and regulatory processes across multiple therapeutic areas.
Job Overview (Quick Details)
| Job Title | Data Surveillance Analyst |
|---|---|
| Company | Parexel |
| Location | India (Remote) |
| Employment Type | Full-Time |
| Department | Clinical Trials / Data Surveillance |
| Experience Required | 2+ Years |
| Education | Life Sciences / Pharmacy / Data Analytics |
| Salary | As per company norms |
| Job ID | R0000039829 |
Job Location & Employment Type
- Location: Remote (Work from anywhere in India)
- Employment Type: Full-time
Open Positions / Department Details
- Department: Clinical Data Surveillance / Risk-Based Monitoring
- Role focuses on centralized monitoring, data analysis, and quality oversight in clinical trials
- Involves collaboration with global teams and technology platforms
Key Roles & Responsibilities
Data Surveillance Planning & Setup
- Assist in creating Data Surveillance Plans (DSPs) for clinical studies
- Define Key Risk Indicators (KRIs) and Quality Tolerance Limits (QTLs)
- Configure central monitoring tools such as CluePoints platform
- Set up data mappings, statistical parameters, and monitoring metrics
Data Analysis & Review
- Perform regular data reviews using surveillance technologies
- Identify trends, inconsistencies, and outliers in clinical trial data
- Analyze operational and scientific data for quality assessment
- Document findings in tracking systems and reports
Risk Identification & Issue Management
- Detect potential data quality issues and compliance risks
- Escalate critical findings to relevant stakeholders
- Recommend corrective actions and follow-up strategies
- Collaborate with teams to resolve data discrepancies
Reporting & Documentation
- Prepare Central Monitoring Reports
- Maintain proper documentation of findings and actions
- Support issue tracking using systems like CluePoints and Veeva Vault
- Ensure compliance with regulatory and internal guidelines
Team Collaboration & Meetings
- Participate in internal and external data surveillance meetings
- Present findings and insights to project teams
- Work closely with data, clinical, and technology teams
- Support decision-making processes with data insights
Compliance & Quality Assurance
- Ensure adherence to ICH-GCP guidelines and regulatory standards
- Maintain awareness of global clinical trial regulations
- Support audits and inspections when required
- Follow SOPs and study-specific requirements
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or Data Analytics
- Equivalent qualification in clinical, technology, or business fields may be considered
Experience
- Minimum 2 years of experience in:
- Clinical research
- Data management
- Central monitoring or data surveillance
- Experience in Risk-Based Monitoring (RBM) is preferred
- Exposure to adaptive trial designs is an advantage
Skills Required
- Strong data analysis and interpretation skills
- Knowledge of centralized monitoring techniques
- Basic understanding of SDTM domains and clinical data standards
- Basic programming knowledge in SAS or SQL
- Proficiency in tools like CTMS, EDMS, and MS Office
- Excellent communication and presentation skills
- Strong problem-solving and critical thinking ability
- Ability to work independently and manage multiple tasks
- Team collaboration skills in global environments
Salary & Benefits
- Salary: As per company norms
- Additional benefits may include:
- Remote working flexibility
- Exposure to global clinical trial projects
- Career growth in data science and clinical research
- Learning opportunities in advanced monitoring technologies
Selection Process
The hiring process generally includes:
- Application screening
- HR discussion
- Technical/data analysis interview
- Final round interview
How to Apply
- Interested candidates should apply via the official Parexel careers portal
- Use Job ID: R0000039829 while searching
- Submit an updated resume with relevant experience in clinical data and monitoring
Important Dates
- Application Deadline: Not specified
Why Apply for This Pharma Job?
- Opportunity to work in advanced data-driven clinical trials
- Exposure to centralized monitoring and risk-based methodologies
- Work with global teams and cutting-edge technologies
- Flexible remote work environment
- Strong career growth in clinical data analytics and monitoring
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with Parexel or any recruiter. We do not charge any fees for job updates. Candidates are advised to verify job details from official sources before applying.
Final Call-to-Action
Interested candidates should apply immediately to secure this opportunity and build a strong career in clinical data surveillance and analytics.
