Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Clinical Data Analyst II
Job ID R0000044587 Hyderabad, Telangana, IndiaJob Summary
We are seeking an experienced Clinical Data Analyst with 4+ years of clinical data management experience to support data review, data cleaning, study build activities, vendor reconciliations, and database lock processes across global clinical trials. The role will be responsible for reviewing clinical data listings, managing data discrepancies, supporting CRF (Case Report Forms) and edit check development, conducting UAT (User Acceptance Testing) activities, reviewing complex external data sources, and ensuring compliance with GCP and regulatory requirements. The successful candidate will collaborate with cross-functional teams, mentor junior CDM (Clinical Data Management) staff, and contribute to high-quality study delivery across therapeutic areas such as Oncology, Hematology, Cardiovascular, Fibrosis, and Cell Therapy.
Skillsets
- Minimum 4+ years of experience in Clinical Data Review and Clinical Data Management.
- Hands-on experience with Medidata RAVE and other EDC (Electronic Data Capture) systems.
- Experience supporting study build activities, including CRF design, edit checks, and integrations.
- Experience performing UAT during study build and validation phases.
- Strong experience in vendor reconciliation and external data review.
- Experience with database lock activities, including CRF freeze and lock processes.
- Knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
- Experience working within Veeva Vault and eTMF environments.
- Experience in Oncology, Hematology, Cardiovascular, Fibrosis, and/or Cell Therapy studies preferred.
- CCDM Certification is advantageous.
- Stable employment history with tenure of at least one year with previous employers or a valid explanation for transitions.
Qualification
Bachelor's Degree in Life Sciences, Pharmacy, Clinical Research, Biotechnology, or a related field.
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