Parexel Hiring Clinical Data Analyst I
About the Company:
PAREXEL is seeking a Clinical Data Analyst I with 6 months to 1 year of experience in clinical data management. This role involves data validation, data management, user acceptance testing, and ensuring compliance with ICH/GCP guidelines.
Position Name:
Clinical Data Analyst I
Organization:
Parexel
Location:
Hyderabad, Bengaluru, SAS Nagar (Mohali), Punjab, India
Salary:
₹4.5 Lakhs to ₹10.0 Lakhs per annum
Qualifications:
- B.Pharm
- M.Pharm
- Pharm.D
- MSc
- BSc
- Lifesciences
Experience:
0 years / Freshers – 1 year
Key Responsibilities:
| Task | Description |
|---|---|
| Data Validation (Cleaning) | Lead data cleaning and review activities, manage queries, and perform manual/SAS listing reviews. Support external vendor data reconciliation. |
| Data Management Documents/Plans | Set up data management documents ensuring proper documentation per SOPs and ICH/GCP guidelines. |
| Study Start-Up Activities and UAT | Lead or perform user acceptance testing on clinical database setups, review protocols, and EDC entry screens. |
| Data Tracking and Entry | Track and review case report forms (CRFs), support data entry as needed. |
| Project Quality Management & Compliance | Ensure compliance with SOPs, ICH/GCP guidelines, lead QC activities on databases/patient data as per business needs. |
| Training | Maintain training compliance per job roles assigned, address training needs as per development goals identified. |
Skills Required:
- Strong problem-solving skills and logical reasoning
- Commitment to first-time quality with a methodical, analytical, and accurate approach
- Time management and prioritization skills
- Ability to work collaboratively within a team environment
- Good interpersonal, oral, and written communication skills
- Learning ability and knowledge-sharing approach
- Flexible attitude towards work assignments and new learning
- Accountability relative to key accountabilities in the job description
- Written and oral fluency in English
Knowledge and Experience:
- Technical aptitude with awareness or prior experience in Microsoft Office Products
- Basic understanding of data management processes and data validation flow
- Basic understanding of ICH-GCP Guidelines, local regulatory requirements, PAREXEL SOPs, and study-specific procedures
- Basic knowledge of Clinical Data Management Systems (e.g., InForm, Rave, Veeva, Datalabs, ClinBase)
- Understanding of Clinical Study Team roles within Data Management
- Experience in the clinical research industry
- Basic knowledge of medical terminology and coding dictionaries (e.g., MedDRA & WHODRUG)
- Basic knowledge of data management operational processes and tasks during study start-up, conduct, and close-out
- Basic knowledge of database setup activities, including database configuration specifications and setup of data validation