Parexel is hiring for the position of Clinical Data Analyst I in Hyderabad, India. The role is designed for professionals with experience in clinical data management, data review, data cleaning, query management and clinical trial database activities.
The position requires at least 2 years of experience in Clinical Data Management within a CRO, pharmaceutical or biotechnology environment. Candidates with hands-on experience in EDC systems, particularly Medidata RAVE or Oracle Clinical, may be suitable for this opportunity.
The role also involves vendor data reconciliation, clinical data listings review, CRF freeze and lock activities, User Acceptance Testing (UAT), eTMF documentation and Veeva Vault management.
Parexel Clinical Data Analyst I – Job Highlights
| Particular | Details |
|---|---|
| Company | Parexel |
| Job Title | Clinical Data Analyst I |
| Location | Hyderabad, India |
| Job Type | Full Time |
| Experience | 2+ Years |
| Qualification | Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research or related discipline |
| Department | Clinical Data Management |
| Key Areas | Data Review, Data Cleaning, Query Management, Reconciliation, Database Lock |
| Preferred EDC | Medidata RAVE, Oracle Clinical |
| Documentation Tools | Veeva Vault, eTMF |
| Requisition ID | R0000046545 |
| Salary / CTC | Not specified |
About Parexel
Parexel is a global clinical research organization that supports pharmaceutical, biotechnology and healthcare companies throughout clinical development and related activities.
Its work spans clinical trials, regulatory services, consulting and market access. Clinical data management is an important part of ensuring that clinical trial information is reviewed, cleaned and maintained according to applicable quality and regulatory requirements.
Job Description
The Clinical Data Analyst I will support clinical trial data management activities, with a focus on data review, data cleaning, query resolution and reconciliation of external or vendor-provided data.
The selected professional will work with clinical data listings, EDC systems and clinical data review tools. The role also includes supporting database freeze and lock activities, UAT and study documentation.
The position requires collaboration with internal teams, external stakeholders and study partners to identify and resolve data discrepancies and maintain accurate clinical trial records.
Clinical Data Analyst I – Role Overview
The role covers several stages of clinical data review and study database activities, including:
- Clinical data review
- Data cleaning
- Clinical data listings review
- Query management
- Discrepancy resolution
- Vendor data reconciliation
- Local laboratory data review
- External data reconciliation
- CRF freeze and database lock
- UAT
- Study documentation
- Veeva Vault and eTMF management
Educational Qualification
Candidates should have a Bachelor’s degree in one of the following or a related scientific field:
- Life Sciences
- Pharmacy
- Biotechnology
- Clinical Research
- Related scientific discipline
Experience Requirements
Candidates should have:
- Minimum 2+ years of experience in Clinical Data Management.
- Experience within a CRO, pharmaceutical or biotechnology organization.
- Practical experience with clinical trial data review and cleaning.
- Experience with query management and discrepancy resolution.
- Experience with vendor data reconciliation.
- Exposure to database freeze and lock activities.
Clinical Data Management Skills
The position requires knowledge and practical experience in:
Clinical Data Review
- Reviewing clinical data listings.
- Identifying inconsistencies and discrepancies.
- Checking clinical data for accuracy and completeness.
- Supporting data-cleaning activities.
Query Management
- Identifying data discrepancies.
- Raising and managing queries.
- Following up on outstanding data issues.
- Supporting resolution of data inconsistencies.
Vendor and External Data Reconciliation
The role includes reconciliation activities involving:
- Vendor-provided data
- Local laboratory data
- Other external clinical data sources
Candidates should understand the importance of comparing external data with clinical trial data and resolving discrepancies.
CRF Freeze and Database Lock
The Clinical Data Analyst will support:
- CRF freeze activities.
- Database lock preparation.
- Data review before lock.
- Identification and resolution of outstanding issues.
- Activities associated with final clinical data readiness.
Key Responsibilities
Clinical Data Review and Cleaning
The selected candidate will:
- Review clinical data listings.
- Identify potential data discrepancies.
- Support data-cleaning activities.
- Ensure clinical data is reviewed according to study requirements.
- Work with relevant teams to resolve identified issues.
Query Management
Responsibilities include:
- Manage clinical data queries.
- Track outstanding discrepancies.
- Coordinate with appropriate stakeholders for resolution.
- Follow queries through to closure.
- Support accurate and timely data cleaning.
Vendor Data Reconciliation
The role involves:
- Reviewing vendor data.
- Supporting local laboratory data review.
- Reconciling external data with clinical trial information.
- Identifying discrepancies between different data sources.
- Coordinating resolution with internal and external stakeholders.
User Acceptance Testing
The Clinical Data Analyst may participate in User Acceptance Testing (UAT) activities involving:
- Clinical data listings
- Screens
- Edit checks
- Other clinical data review functionality
The role requires attention to detail when identifying issues during testing and supporting their resolution.
Study Documentation
The selected professional will maintain clinical study documentation, including activities related to:
- Veeva Vault
- Electronic Trial Master File (eTMF)
- Study documentation
- Clinical data management records
Accurate and timely documentation is an important part of the position.
Tools and Systems
Electronic Data Capture Systems
Experience with the following systems is relevant:
- Medidata RAVE – preferred
- Oracle Clinical
Clinical Data Review Tools
The vacancy mentions:
- J-Review
- Spotfire
Documentation Platforms
Candidates should be familiar with:
- Veeva Vault
- eTMF
Microsoft Applications
Knowledge of Microsoft tools including:
- Microsoft Office
- Microsoft Project
- PowerPoint
is relevant to the position.
Regulatory and Compliance Knowledge
Candidates should have a working understanding of:
- ICH-GCP
- Clinical trial regulations
- Clinical research processes
- Regulatory guidelines
- 21 CFR Part 11
- Clinical Data Management processes
This knowledge is important for maintaining data quality and compliance throughout clinical studies.
Cross-Functional Collaboration
The Clinical Data Analyst will work with different internal and external stakeholders involved in clinical research.
The role requires:
- Strong stakeholder communication.
- Coordination with clinical data teams.
- Collaboration with vendors.
- Interaction with external stakeholders.
- Timely escalation and resolution of data issues.
- Effective communication during study activities.
Required Professional Skills
Candidates should demonstrate:
- Strong attention to detail.
- Clinical data review capability.
- Data-cleaning knowledge.
- Query management skills.
- Analytical and problem-solving ability.
- Good organizational skills.
- Strong written communication.
- Strong verbal communication.
- Stakeholder management.
- Ability to work collaboratively.
- Understanding of clinical trial processes.
- Ability to manage multiple study-related activities.
Work Location
- Location: Hyderabad, India
- Job Type: Full Time
- Function: Clinical Data Management
- Requisition ID: R0000046545
The available vacancy information does not specify whether the position is office-based, hybrid or remote.
Salary / CTC
The salary or CTC for the Parexel Clinical Data Analyst I position has not been specified in the available vacancy information.
Candidates should confirm compensation and employment terms through the official recruitment process.
Selection Process
The detailed selection process has not been provided in the vacancy information.
Candidates may be assessed based on their Clinical Data Management experience, EDC knowledge, data review skills, reconciliation experience, regulatory knowledge and ability to work with cross-functional teams.
How to Apply for Parexel Clinical Data Analyst I
Interested and eligible candidates should submit their application through Parexel’s official recruitment platform.
Candidates should ensure that their resume clearly highlights relevant Clinical Data Management, EDC, data review, reconciliation and database lock experience.
Important Details Before Applying
- The company is Parexel.
- The position is Clinical Data Analyst I.
- The job location is Hyderabad, India.
- The vacancy requires 2+ years of Clinical Data Management experience.
- Experience in a CRO, pharmaceutical or biotechnology environment is required.
- A Bachelor’s degree in a relevant scientific discipline is required.
- Medidata RAVE experience is preferred.
- Oracle Clinical experience is also relevant.
- Experience with Veeva Vault and eTMF is preferred.
- The role includes data review, cleaning, query management and reconciliation.
- CRF freeze and database lock activities are part of the position.
- UAT experience is relevant.
- The requisition ID is R0000046545.
- Salary/CTC has not been disclosed.
Frequently Asked Questions
1. What is the job title at Parexel?
The position is Clinical Data Analyst I.
2. Where is the job located?
The position is based in Hyderabad, India.
3. How much experience is required?
Candidates should have at least 2+ years of experience in Clinical Data Management.
4. What educational qualification is required?
A Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research or a related scientific discipline is required.
5. Is Medidata RAVE experience required?
Medidata RAVE experience is preferred. Oracle Clinical is also listed among the relevant EDC systems.
6. What clinical data activities are involved?
The role includes data review, data cleaning, query management, clinical data listings review, vendor reconciliation, external data review and database lock activities.
7. Does the role involve UAT?
Yes. The position includes User Acceptance Testing for listings, screens and edit checks.
8. Is Veeva Vault experience useful?
Yes. Experience with Veeva Vault and eTMF documentation is preferred.
9. What regulatory knowledge is required?
Candidates should understand ICH-GCP, clinical research regulations, regulatory guidelines and 21 CFR Part 11.
10. What tools are mentioned in the vacancy?
The vacancy mentions Medidata RAVE, Oracle Clinical, J-Review, Spotfire, Veeva Vault, eTMF, Microsoft Office, Microsoft Project and PowerPoint.
11. What is the requisition ID?
The requisition ID is R0000046545.
12. What is the salary for this position?
The salary or CTC has not been specified in the available vacancy information.
Important Note
Recruitment requirements, eligibility criteria, work arrangements, compensation and other employment conditions may change. Candidates should verify the latest vacancy details on Parexel’s official careers platform before applying and should rely on the employer’s official recruitment communication for final employment terms.