Job Title: Clinical Data Services Associate
Company: Accenture
Location: Mumbai
Job Type: Full-Time
Experience Required: 1–3 Years
Qualification: B.Pharm / BE / M.Sc
About the Role
Accenture is hiring a Clinical Data Services Associate to support clinical trial data management and SAS-based clinical data operations. The role involves data integration, validation, standardization, and management of clinical research data to ensure high-quality datasets for regulatory submissions and clinical study analysis. This opportunity is ideal for candidates with SAS knowledge and an interest in clinical research and data management.
Key Responsibilities
Clinical Data Management
Support collection, validation, and management of clinical trial data.
Ensure data accuracy, consistency, and completeness across studies.
Assist in maintaining clinical databases and metadata repositories.
Support data cleaning and query resolution activities.
SAS Programming Support
Work with Base SAS for clinical data processing and analysis.
Assist in generating datasets, reports, and data outputs.
Support data integration and standardization activities.
Maintain data quality and compliance standards during programming activities.
Data Integration & Validation
Organize and standardize clinical research data from multiple sources.
Perform validation checks and identify data discrepancies.
Support cross-study data analysis and advanced safety analysis activities.
Ensure compliance with clinical data standards and project requirements.
Quality & Compliance
Follow SOPs, regulatory guidelines, and quality standards.
Ensure clinical datasets meet regulatory and internal requirements.
Support audit readiness and documentation activities.
Maintain accurate records of data management activities.
Team Collaboration
Work closely with clinical data managers, biostatisticians, and study teams.
Communicate data issues and support timely resolution.
Participate in project meetings and team discussions.
Adapt to shifting priorities and project timelines.
Required Skills
Base SAS
Clinical Data Management
Clinical Trial Data Handling
Data Validation
Data Integration
Clinical Domain Knowledge
Data Quality Review
Documentation Management
Analytical Thinking
Written & Verbal Communication
Team Collaboration
Attention to Detail
Preferred Qualifications
Knowledge of CDISC, SDTM, or ADaM standards.
Exposure to clinical research, CRO, or pharmaceutical environments.
Understanding of GCP and clinical trial processes.
Familiarity with clinical databases and reporting tools.
Uttar Pradesh :
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