Accenture is inviting applications for the position of Clinical Data Svs Analyst in Bengaluru, Karnataka. The role is aligned with the Life Sciences R&D vertical and focuses on clinical data services, SAS programming, statistical programming deliverables, quality control, dataset validation, and clinical trial documentation.
Candidates with any graduation qualification and 3–5 years of experience can review the requirements for this full-time opportunity.
Job Details
| Particulars | Details |
|---|---|
| Company | Accenture |
| Job Title | Clinical Data Svs Analyst |
| Job Location | Bengaluru, BDC9A |
| Employment Type | Full Time |
| Qualification | Any Graduation |
| Experience | 3–5 Years |
| Required Skill | Clinical Data Services – Medical Monitoring |
| Job Requisition ID | AIOC-S01639553 |
| Shift | Rotational shifts may be required |
Position: Clinical Data Svs Analyst
The selected candidate will support clinical trial data management and statistical programming activities, including developing SAS programs, validating datasets, performing quality control checks, and ensuring compliance with applicable standards and procedures.
Roles and Responsibilities
- Analyse and resolve moderately complex problems using established methods and procedures.
- Coordinate between study teams, offshore teams, and onshore or client stakeholders.
- Collaborate with Senior Statistical Programmers, study leads, and programmers to support study execution.
- Perform quality control checks for standard and non-standard safety and efficacy deliverables.
- Review approved protocols, study setup documents, submission documents, and output specifications.
- Develop SAS programs and execute standard macros to generate SDTM-like datasets, SDTM datasets, tables, listings, figures, and trial-specific outputs.
- Perform developer testing and validate datasets and outputs against defined standards.
- Apply programming and data standards to improve consistency and efficiency across studies.
- Maintain project, validation, and programming documentation according to SOP requirements.
- Follow applicable client and Accenture SOPs and quality guidelines.
- Mentor new hires, support onboarding, and address technical or process-related queries.
- Conduct Service Readiness Assessments for new resources.
- Support resource management, operational reporting, and daily study activities.
- Complete assigned training and support organisational and Business Excellence initiatives.
Eligibility and Qualifications
- Educational Qualification: Any graduation.
- Experience: 3–5 years.
- Ability to work independently on routine tasks and contribute to individual or team deliverables.
Required Skills
- Clinical data services
- SAS programming
- Statistical programming support
- SDTM datasets and clinical trial outputs
- Quality control and dataset validation
- Safety and efficacy deliverables
- Clinical study documentation
- Standard Operating Procedures (SOPs) and quality compliance
- Problem-solving skills
- Written and verbal communication
- Adaptability and flexibility
- Team collaboration and stakeholder coordination
