Parexel has announced a new opening for the position of Clinical Data Analyst II in Hyderabad. This opportunity is suitable for experienced clinical data management professionals looking to work on global clinical trials and strengthen their expertise in clinical data review, study build, EDC systems, vendor reconciliation, UAT, and database lock activities.
The Parexel Clinical Data Analyst II job involves supporting high-quality clinical trial data management across therapeutic areas that may include Oncology, Hematology, Cardiovascular, Fibrosis, and Cell Therapy.
Candidates with a Bachelor’s degree in Life Sciences, Pharmacy, Clinical Research, Biotechnology, or a related discipline and at least four years of relevant clinical data management experience can review the eligibility requirements and apply online.
About Parexel
Parexel is a global clinical research organization supporting the development and commercialization of medicines and therapies. Its services span clinical trials, regulatory affairs, consulting, market access, and other areas of drug development.
Through its clinical research operations, Parexel works with pharmaceutical and biotechnology organizations to support the development of therapies for patients worldwide.
Job Responsibilities
As a Clinical Data Analyst II at Parexel, the selected candidate may be responsible for:
- Performing clinical data review and data cleaning activities across clinical studies.
- Reviewing clinical data listings and identifying data inconsistencies or discrepancies.
- Managing and resolving clinical data queries in accordance with study requirements.
- Supporting study build activities, including CRF design and development.
- Supporting the development and validation of edit checks and study integrations.
- Conducting User Acceptance Testing (UAT) during study build and validation.
- Reviewing and reconciling external and vendor clinical trial data.
- Handling complex external data sources and identifying reconciliation issues.
- Supporting database lock activities, including CRF freeze and CRF lock processes.
- Maintaining appropriate clinical data management and study documentation.
- Working within Veeva Vault and eTMF environments.
- Ensuring clinical data management activities comply with ICH-GCP and applicable regulatory requirements.
- Collaborating with data managers and other cross-functional clinical trial stakeholders.
- Supporting high-quality and timely study deliverables.
- Providing guidance and mentoring support to junior clinical data management team members when required.
Eligibility & Qualifications
Candidates interested in the Parexel Clinical Data Analyst II Hyderabad vacancy should meet the following requirements:
Educational Qualification
A Bachelor’s degree in one of the following or a related discipline:
- Life Sciences
- Pharmacy
- Clinical Research
- Biotechnology
- Related scientific or healthcare disciplines
Experience
Candidates should have 4+ years of relevant experience in Clinical Data Management and Clinical Data Review.
Parexel also indicates a preference for candidates with a stable employment history, typically including at least one year of tenure with previous employers, or a reasonable explanation for employment transitions.
Key Skills Required
Candidates should ideally possess experience in:
- Clinical Data Management
- Clinical Data Review
- Clinical Data Cleaning
- Clinical Data Listings Review
- Data Discrepancy Management
- Query Management
- Medidata RAVE
- Electronic Data Capture (EDC) systems
- CRF Design
- Edit Check Development
- Study Build Activities
- User Acceptance Testing (UAT)
- Vendor Data Reconciliation
- External Data Review
- Database Lock
- CRF Freeze and Lock
- Veeva Vault
- eTMF
- ICH-GCP
- Clinical Trial Processes
- Regulatory Compliance
Experience in Oncology, Hematology, Cardiovascular, Fibrosis, or Cell Therapy clinical trials is preferred.
CCDM certification may provide an additional advantage but is not stated as a mandatory qualification.
Why Consider This Parexel Clinical Data Management Job?
This role provides experienced clinical data professionals with an opportunity to contribute to global clinical research programs while developing expertise across multiple aspects of the clinical data lifecycle.
Potential professional benefits include:
- Exposure to global clinical trials
- Experience with complex clinical datasets
- Hands-on work with Medidata RAVE and EDC platforms
- Exposure to study build and validation processes
- Experience with CRF development and edit checks
- Vendor and external data reconciliation exposure
- Database lock experience
- Cross-functional collaboration
- Exposure to specialized therapeutic areas
- Opportunity to mentor junior CDM professionals
- Career development within clinical research and data management
Salary
Parexel has not disclosed the salary for this vacancy in the provided job posting.
For informational purposes, an estimated market-aligned salary range for an experienced Clinical Data Analyst/CDM professional in India may be approximately:
₹7,00,000 – ₹14,00,000 per year
This is an editorial estimate for informational and structured-data purposes and is not an official salary range announced by Parexel. Actual compensation may vary according to experience, skills, location, internal compensation structure, and other factors.
How to Apply
