Parexel is hiring for the Clinical Data Analyst I position in Hyderabad, India. This opportunity is suitable for life sciences and pharmacy professionals with at least 2 years of Clinical Data Management experience who want to build their careers in clinical research and data operations.

The Parexel Clinical Data Analyst I job in Hyderabad involves clinical trial data review, data cleaning, query management, vendor data reconciliation, CRF freeze and database lock activities, User Acceptance Testing (UAT), and clinical study documentation.

Candidates with hands-on experience in Medidata RAVE, Oracle Clinical, J-Review, Spotfire, Veeva Vault, eTMF, or similar clinical data management systems may be particularly relevant for this position.

Parexel is a global clinical research organization supporting pharmaceutical and biotechnology companies across clinical development, regulatory, consulting, and market access activities.

Job Overview

Key Responsibilities

As a Clinical Data Analyst I at Parexel, selected candidates may be responsible for:

• Reviewing clinical trial data and performing routine data cleaning activities.
• Reviewing clinical data listings to identify missing, inconsistent, or potentially erroneous data.
• Creating, managing, and resolving clinical data queries and discrepancies.
• Performing vendor data reconciliation, including local laboratory data review.
• Reviewing and reconciling external clinical trial data.
• Supporting CRF freeze and lock activities.
• Participating in clinical database lock processes.
• Conducting User Acceptance Testing (UAT) for data listings, screens, and edit checks.
• Supporting clinical data review activities using appropriate data review tools.
• Maintaining required study documentation within Veeva Vault and eTMF.
• Working with cross-functional teams and internal and external stakeholders.
• Supporting accurate and timely completion of Clinical Data Management activities.
• Following applicable clinical research procedures, regulatory requirements, and data quality standards.

Qualification and Eligibility

Candidates interested in the Parexel Clinical Data Analyst I vacancy should meet the following requirements:

Educational Qualification

A Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related scientific discipline is required.

Relevant educational backgrounds may include:

• B.Pharm
• B.Sc. Life Sciences
• B.Sc. Biotechnology
• Bachelor’s in Clinical Research
• Other related scientific disciplines

Candidates should verify their exact degree eligibility against Parexel’s official application requirements before submitting an application.

Experience Required

Candidates should have a minimum of 2+ years of Clinical Data Management experience, preferably gained within a CRO, pharmaceutical, or biotechnology environment.

This position is therefore primarily intended for experienced Clinical Data Management professionals rather than fresh graduates.

Skills Required for Parexel Clinical Data Analyst I

Applicants should have relevant knowledge or hands-on experience in:

• Clinical Data Management
• Clinical Data Review
• Data Cleaning
• Clinical Data Listings Review
• Query Management
• Discrepancy Management
• Vendor Data Reconciliation
• Local Lab Data Review
• External Data Reconciliation
• CRF Freeze and Lock
• Database Lock Activities
• User Acceptance Testing (UAT)
• Edit Check Testing
• eTMF Documentation
• Veeva Vault
• Clinical Data Workbench
• EDC Systems
• Clinical Trial Processes
• ICH-GCP
• Regulatory Guidelines
• 21 CFR Part 11
• Stakeholder Management
• Cross-functional Collaboration

Strong written and verbal communication skills are also important because Clinical Data Management teams frequently coordinate with multiple study stakeholders.

Tools and Systems

Experience with the following Clinical Data Management tools may strengthen a candidate’s profile:

EDC Systems

• Medidata RAVE – Preferred
• Oracle Clinical

Data Review Tools

• J-Review
• Spotfire

Clinical Documentation

• Veeva Vault
• eTMF

Additional Tools

• Microsoft Office Suite
• Microsoft Project
• Microsoft PowerPoint

Candidates do not necessarily need to list every tool unless they have genuine working knowledge or hands-on experience with it.

Why Consider a Clinical Data Management Career at Parexel?

The Clinical Data Analyst I role at Parexel provides exposure to important stages of clinical trial data management, including data review, discrepancy resolution, reconciliation, UAT, and database lock.

Potential professional benefits include:

• Experience working within a global clinical research organization.
• Exposure to clinical trial data management processes.
• Hands-on involvement with EDC and clinical data review systems.
• Experience with vendor and external data reconciliation.
• Exposure to database freeze and lock activities.
• Cross-functional collaboration with clinical research stakeholders.
• Opportunities to strengthen knowledge of GCP and regulated clinical trial processes.
• Career development opportunities within Clinical Data Management and broader clinical research functions.

Specific compensation, employee benefits, insurance, leave policies, and other employment benefits should be confirmed directly with Parexel during the recruitment process.

Who Should Apply?

This position may be particularly relevant for professionals currently working as:

• Clinical Data Coordinator
• Clinical Data Management Associate
• Clinical Data Associate
• Clinical Data Analyst
• Clinical Data Reviewer
• Data Management Associate
• Clinical Data Management Executive

Candidates with approximately 2 or more years of relevant CDM experience and hands-on exposure to clinical data review, EDC systems, query management, reconciliation, or database lock activities should consider applying.

How to Apply

Application Link