Clinical Data Analyst II

Parexel; India; On-site; INR 900,000 - 1,300,000; Full time

Job summary

Parexel is seeking an experienced Clinical Data Analyst with 4+ years in clinical data management to support data review, cleaning, and study build activities across global trials. The role includes CRF design, edit checks, UAT, external data reviews, and collaboration with cross-functional teams to deliver high-quality studies.

The candidate will mentor junior CDM staff, work in Oncology, Hematology, and other domains, and ensure compliance with GCP and regulatory requirements.

Qualifications

• 4+ years of clinical data management and data review experience.
• Hands-on Medidata RAVE and other EDC systems experience.
• Experience with CRF design, edit checks, and data validation; UAT exposure.

Responsibilities

• Review listings, clean data, and support data review across trials.
• Assist CRF design, edit checks, and data validation activities.
• Lead UAT during study builds and ensure data quality.
• Mentor junior CDM staff and collaborate with cross-functional teams.
• Perform vendor reconciliations and support database lock processes.

Skills

Clinical Data Review

Clinical Data Management

Medidata RAVE

EDC Systems

CRF Design

UAT

Vendor Reconciliation

Regulatory Knowledge

GCP Awareness

Veeva Vault

eTMF

Education

Bachelor's Degree in Life Sciences or related field

Tools

Medidata RAVE

Veeva Vault

eTMF platforms

Job description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Job 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.