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Clinical Data Svs Associate

Accenture
1-3 years
INR 4.5 LPA – 7.5 LPA
Bangalore, India
1 June 23, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

CLINICAL DATA SERVICES ASSOCIATE

Company: Accenture
Location: Bengaluru, India
Job ID: AIOC-S01648538
Department: Life Sciences R&D – Clinical Data Services
Employment Type: Full Time

JOB OVERVIEW

The Clinical Data Services Associate will support clinical research and clinical trial operations by managing, validating, reviewing, and monitoring clinical data. The role focuses on ensuring data quality, regulatory compliance, protocol adherence, and supporting medical monitoring activities for pharmaceutical and biotechnology clients.

KEY RESPONSIBILITIES

• Clinical Data Management

  • Manage and process clinical trial data.

  • Support data collection, validation, and quality review activities.

  • Ensure accuracy, completeness, and consistency of clinical trial data.

  • Maintain data integrity throughout the clinical study lifecycle.

  • Support clinical database maintenance and updates.

• Medical Monitoring Support

  • Provide medical expertise for clinical trial oversight.

  • Assist in identification and review of safety concerns.

  • Support review and validation of protocol requirement specifications.

  • Ensure protocol compliance during study execution.

  • Escalate potential medical or safety issues as required.

• Clinical Trial Support

  • Assist in monitoring clinical trial activities.

  • Support clinical research teams in data-related activities.

  • Review study documentation and clinical records.

  • Participate in quality checks and compliance reviews.

  • Contribute to successful trial execution and delivery.

• Regulatory Compliance

  • Follow applicable SOPs and regulatory guidelines.

  • Ensure compliance with clinical research standards.

  • Support audit and inspection readiness activities.

  • Maintain proper documentation and records.

  • Adhere to data privacy and confidentiality requirements.

• Data Analysis & Validation

  • Review and validate clinical data.

  • Identify discrepancies and data quality issues.

  • Support resolution of data queries.

  • Generate reports and summaries as required.

  • Ensure reliable data is available for safety and efficacy evaluations.

• Daily Operations

  • Solve routine operational issues using established guidelines.

  • Work closely with team members and supervisors.

  • Meet assigned productivity and quality targets.

  • Manage multiple priorities effectively.

  • Work in rotational shifts if required.

REQUIRED QUALIFICATIONS

  • Bachelor of Engineering (BE)

  • Bachelor of Pharmacy (B.Pharm)

  • Master of Pharmacy (M.Pharm)

EXPERIENCE

1–3 Years of Experience

  • Experience in Clinical Data Management, Clinical Research, Pharmacovigilance, Medical Monitoring, or Clinical Operations preferred.

  • Understanding of clinical trial processes is advantageous.

  • Knowledge of GCP and clinical research regulations is beneficial.