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Clinical Data Svs New Associate

Accenture
Accenture
0-2 years
Not Disclosed
Bengaluru, India
10 April 21, 2026
Job Description
Job Type: Full Time Education: B.sc/ M.sc/ B.Pharm/ M.Pharm/ Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Job Title: Clinical Data Services New Associate

Skill Area: Clinical Data Operations – Clinical Data Management

Company: Accenture

Location: Bengaluru

Experience Required: 0–1 Year


Educational Qualifications

  • MSc

  • Bachelor of Pharmacy (B.Pharm)

  • Master’s Degree in Life Sciences


Role Overview

The Clinical Data Services New Associate will be part of the Life Sciences R&D vertical, supporting clinical research through effective data management. The role focuses on ensuring high-quality, accurate, and compliant clinical trial data to support evaluation of treatment safety and efficacy.


About the Organization

Accenture is a global professional services company specializing in digital, cloud, and security services. With operations in over 120 countries, it provides services across Strategy & Consulting, Technology, and Operations to clients across multiple industries, including Life Sciences.


Key Responsibilities

1. Clinical Data Management

  • Manage and support clinical trial data collection, validation, and storage

  • Ensure data accuracy, integrity, and compliance with regulatory standards

  • Assist in data analysis to support clinical research outcomes

2. Operational Support

  • Work within Clinical, Pharmacovigilance & Regulatory sub-offerings

  • Support clinical trial conduct, management, and reporting activities

  • Follow established processes and guidelines for data operations

3. Task Execution

  • Solve routine problems using predefined procedures and guidelines

  • Execute tasks based on detailed instructions from supervisors

  • Ensure timely completion of assigned work

4. Team Collaboration

  • Collaborate with team members and report to direct supervisors

  • Work as an individual contributor within a defined scope

  • Support team goals and project deliverables

5. Compliance & Quality

  • Ensure adherence to regulatory standards and organizational processes

  • Maintain high-quality data standards for clinical research


Work Environment

  • May require working in rotational shifts

  • Role involves working under supervision with a structured workflow


Required Skills & Competencies

  • Ability to meet deadlines

  • Ability to work under pressure

  • Strong teamwork and collaboration skills

  • Attention to detail and accuracy


Additional Information

  • Equal Employment Opportunity: Hiring decisions are based on merit without discrimination

  • Candidates are not required to pay any fees during the hiring process

  • For suspicious job-related communications, contact the company through official channels


About Clinical Data Operations

Clinical Data Management is a critical function in clinical research that ensures:

  • Accurate data collection and validation

  • Reliable data integration and analysis

  • Compliance with regulatory standards

  • Support for evaluation of treatment safety and efficacy