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Clinical Data Svs Associate

Accenture
1-3 years
INR 4.5 LPA – 7 LPA
Mumbai, India
1 June 19, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Clinical Data Services Associate

Location: Mumbai, Maharashtra, India
Company: Accenture
Department: Life Sciences R&D – Clinical Data Services
Employment Type: Full-Time
Shift: Rotational Shifts

Role Summary

The Clinical Data Services Associate is responsible for supporting clinical data management, processing, validation, integration, and reporting activities for global clinical research programs. The role involves working with clinical trial data, ensuring data quality, supporting regulatory compliance, and contributing to the successful delivery of clinical research projects.

This position combines clinical domain knowledge with technical skills in SAS and clinical data systems to support pharmaceutical, biotechnology, and life sciences clients in evaluating the safety and efficacy of medical treatments.

Key Responsibilities

Clinical Data Management & Processing

  • Support end-to-end clinical data management activities.

  • Assist in:

    • Data Collection

    • Data Validation

    • Data Cleaning

    • Data Integration

    • Data Review

    • Data Reporting

  • Ensure clinical trial data is accurate, complete, and reliable.

  • Follow established clinical data management procedures and standards.

Clinical Trial Data Review

  • Review and validate clinical trial datasets.

  • Identify and resolve:

    • Data Discrepancies

    • Missing Information

    • Data Quality Issues

  • Support consistency and integrity of clinical research data.

  • Ensure data readiness for downstream analysis and reporting.

SAS Programming Support

  • Utilize Base SAS for:

    • Data Validation

    • Data Manipulation

    • Data Listings

    • Reporting Activities

  • Support creation and maintenance of clinical data outputs.

  • Assist with quality checks of SAS-generated datasets and reports.

  • Ensure compliance with project-specific programming standards.

Clinical Data Integration

  • Support integration and standardization of clinical research data.

  • Work with clinical databases and metadata repositories.

  • Assist in preparing datasets for:

    • Cross-Study Analysis

    • Safety Analysis

    • Regulatory Reporting

    • Clinical Research Reporting

  • Ensure data structures support analytical and operational requirements.

Data Quality & Compliance

  • Perform quality checks to ensure data accuracy and consistency.

  • Adhere to:

    • Clinical Data Management Standards

    • Regulatory Requirements

    • Client-Specific Processes

    • Organizational Policies

  • Support audit readiness and compliance initiatives.

  • Maintain documentation related to data management activities.

Clinical Research Support

  • Collaborate with teams supporting:

    • Clinical Trials

    • Regulatory Affairs

    • Pharmacovigilance

    • Clinical Operations

  • Assist in evaluating clinical data related to:

    • Safety

    • Efficacy

    • Study Outcomes

  • Contribute to successful execution of clinical research programs.

Operational Support & Problem Solving

  • Resolve routine operational issues using established guidelines and procedures.

  • Escalate complex issues to supervisors when necessary.

  • Complete assigned deliverables within required timelines.

  • Maintain productivity and quality expectations.

Team Collaboration

  • Work as an individual contributor within a structured team environment.

  • Collaborate with:

    • Team Members

    • Supervisors

    • Clinical Data Specialists

    • Project Stakeholders

  • Participate in team discussions and knowledge-sharing activities.

  • Support a collaborative and quality-focused work culture.

Continuous Learning & Development

  • Build expertise in:

    • Clinical Data Management

    • SAS Programming

    • Clinical Research Processes

    • Regulatory Requirements

  • Stay updated with industry trends and best practices.

  • Participate in training and professional development programs.

Required Qualifications

Education

One of the following qualifications:

  • Bachelor of Pharmacy (B.Pharm)

  • Bachelor’s Degree in:

    • Life Sciences

    • Biotechnology

    • Biomedical Sciences

    • Clinical Research

    • Related Scientific Discipline

  • BE (Engineering) in a relevant discipline

  • Master of Science (M.Sc.)

Experience

  • 1–3 years of experience in:

    • Clinical Data Management

    • Clinical Research

    • SAS Programming

    • Life Sciences Operations

  • Fresh graduates with strong SAS and clinical domain knowledge may also be considered.