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Clinical Data Services Associate

Accenture
Accenture
0-2 years
preferred by company
Bangalore, India
1 May 14, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill

Clinical Data Services Associate
Location: Bengaluru, Karnataka, India
Employment Type: Full-Time
Department: Clinical Data Management / Life Sciences / Clinical Research Operations
Experience Required: 0–2 Years (Freshers with relevant qualifications may be considered)


Job Overview

A promising opportunity is available for a Clinical Data Services Associate within the life sciences and clinical research domain. This role is ideal for professionals interested in clinical data management, clinical database programming, electronic data capture (EDC), clinical trial data validation, and regulatory-compliant clinical research operations.

The selected candidate will support clinical research programs by ensuring high-quality clinical trial data management, validation, reporting, and database review processes. This role plays a critical part in maintaining accurate and reliable clinical trial data to support regulatory compliance, medical treatment evaluation, and successful study outcomes.

This position is well-suited for early-career professionals looking to build expertise in clinical data services, life sciences R&D, biopharmaceutical operations, and clinical technology platforms.


Key Responsibilities

Clinical Data Management

  • Support the collection, validation, processing, and management of clinical trial data
  • Ensure accuracy, consistency, and integrity of study data throughout the clinical research lifecycle
  • Assist in maintaining regulatory-compliant clinical data systems and workflows

Clinical Database Programming & Validation

  • Develop and review complex edit checks based on study-specific requirements
  • Support patient profile listings, reports, preprocessing checks, and dataset validation
  • Participate in mapping datasets for data verification and quality control
  • Assist in database testing and validation activities

Clinical EDC Support

  • Support Clinical EDC (Electronic Data Capture) build and design activities
  • Work with clinical systems and tools used for data management and reporting
  • Ensure accurate implementation of study database specifications

Clinical Research Operations

  • Collaborate with internal teams supporting clinical trials, regulatory functions, and research operations
  • Assist in maintaining documentation aligned with clinical quality standards
  • Support delivery of reliable data for safety and efficacy evaluation

Team & Operational Support

  • Resolve routine operational issues by following established processes and guidelines
  • Work closely with direct supervisors and team members
  • Manage assigned tasks with accuracy and within project timelines
  • Adapt to rotational shifts if required by business operations

Required Qualifications

Educational Qualifications
Candidates should hold one of the following:

  • Bachelor of Engineering (BE)
  • Master of Science (MSc)
  • Equivalent qualification in life sciences, clinical research, biotechnology, health sciences, or related disciplines

Required Skills & Competencies

  • Clinical Data Management knowledge
  • Clinical Database Testing experience or understanding
  • Clinical EDC Build familiarity
  • Clinical EDC Design exposure
  • Understanding of clinical trial data workflows
  • Strong analytical and problem-solving skills
  • Ability to manage multiple stakeholders
  • Strong communication and collaboration skills
  • Client relationship management capabilities
  • Ability to work in structured, process-driven environments

Preferred Technical Skills

Experience or familiarity with:

  • Cognos
  • SAS
  • J-Review
  • Clinical database programming tools
  • Clinical trial data validation platforms
  • Electronic Data Capture (EDC) systems
  • Clinical reporting and dataset mapping tools

Experience Requirements

  • 0–2 years of relevant experience preferred
  • Freshers with strong academic backgrounds in clinical research, data management, life sciences, or related fields may apply
  • Prior exposure to clinical trial operations, EDC systems, or clinical database environments will be advantageous