Parexel Hiring Clinical Data Analyst
Are you searching for a Clinical Data Management Job in India? Parexel is hiring a Clinical Data Analyst II to manage, analyze, clean, validate, and reconcile clinical trial data.
The selected candidate will support data-query management, clinical database setup, User Acceptance Testing, database-lock activities, and study documentation. Candidates with relevant Clinical Data Management or clinical research experience are encouraged to apply.
- Job Title: Clinical Data Analyst II
- Company: Parexel
- Job ID: R0000045515
- Category: Data Management
- Primary Location: Bengaluru, India
- Additional Locations: Hyderabad and Remote, India
- Qualification: Bachelor’s degree in Life Sciences or a related discipline
- Experience: Relevant Clinical Data Management or clinical research experience
About Parexel
Parexel is a global clinical research organization that supports pharmaceutical and biotechnology companies throughout the drug-development lifecycle. Its teams contribute to clinical research, regulatory operations, data management, biostatistics, pharmacovigilance, and the development of new therapies.
The company provides professionals with opportunities to work on clinical studies while collaborating with cross-functional teams, clients, and stakeholders in a regulated global environment.
Job Description
The Parexel Clinical Data Analyst II will support the management, analysis, validation, cleaning, and reconciliation of clinical trial data. These activities help advance clinical research objectives and support regulatory submissions.
The position requires strong technical and analytical abilities, excellent attention to detail, and the capacity to work independently. The candidate will also collaborate with cross-functional study teams and contribute to study-start-up support while ensuring compliance with SOPs, applicable regulations, industry standards, and ICH-GCP guidelines.
Key Responsibilities
- Extract, clean, validate, and reconcile clinical trial data collected from different sources.
- Perform clinical data validation and ensure the completeness and accuracy of study data.
- Review manual and system-generated data listings to identify discrepancies.
- Investigate and resolve data inconsistencies.
- Generate, manage, and resolve clinical data queries.
- Support clinical database-lock activities.
- Assist with the preparation and maintenance of Data Management documents.
- Maintain accurate and complete study-related records.
- Conduct User Acceptance Testing for clinical database setups.
- Review study protocols, Case Report Forms, and Electronic Data Capture screens when required.
- Track CRFs and support data-entry activities as needed.
- Ensure adherence to company SOPs, regulatory requirements, and ICH-GCP guidelines.
- Collaborate with cross-functional study teams and client stakeholders.
- Support study-start-up and ongoing data-management activities.
- Mentor junior data analysts.
- Contribute to process-improvement initiatives.
Eligibility Criteria
- Educational Qualification: Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, or a related discipline.
- Experience: Relevant experience in Clinical Data Management or the clinical research industry.
- Primary Location: Bengaluru.
- Additional Work Locations: Hyderabad and remote within India.
Technical Requirements
- Experience working with Clinical Data Management Systems.
- Familiarity with platforms such as Medidata Rave, Veeva, DataLabs, ClinBase, or similar systems.
- Understanding of clinical data-management processes.
- Experience with clinical data cleaning, validation, reconciliation, and query management.
- Knowledge of clinical database-lock activities.
- Familiarity with MedDRA and WHODrug coding dictionaries.
- Basic understanding of SAS.
- Basic knowledge of CDISC standards.
- Good understanding of ICH-GCP guidelines.
- Knowledge of applicable clinical research regulations and industry standards.
- Experience reviewing protocols, CRFs, EDC screens, and clinical data listings is advantageous.
Required Skills
- Strong analytical and problem-solving abilities.
- Excellent attention to detail.
- Commitment to clinical data quality and accuracy.
- Strong written and verbal communication skills.
- Effective time-management and prioritization abilities.
- Ability to work independently.
- Ability to collaborate with cross-functional teams.
- Adaptability to evolving project requirements.
- Willingness to learn new technologies, systems, and processes.
- Ability to manage multiple activities within established timelines.
Why Join Parexel?
The Clinical Data Analyst II role provides an opportunity to contribute directly to the quality and reliability of clinical trial data. Candidates will work alongside clinical research professionals and cross-functional study teams while supporting important data-management activities across the clinical development process.
Professionals can develop practical expertise in clinical databases, data validation, discrepancy management, coding dictionaries, CDISC standards, regulatory compliance, and database-lock activities.
Apply for the Parexel Clinical Data Analyst Job
This Parexel Clinical Data Analyst II job is an excellent opportunity for Life Sciences, Pharmacy, Biotechnology, Nursing, and related graduates with relevant clinical data-management or clinical research experience.
Eligible candidates interested in opportunities in Bengaluru, Hyderabad, or remote locations within India are encouraged to apply at the earliest.
Pharmanika is a career information portal. Candidates should verify the qualifications, experience requirements, work arrangement, application deadline, and other details through the official Parexel job notification before applying.
