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Clinical Data Associate I/Ii

2-4 years
Not Disclosed
10 July 29, 2025
Job Description
Job Type: Remote 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, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Clinical Data Associate I/II – Remote (Bangalore)

Job Summary

Join a leading global CRO and contribute to breakthrough drug development as a Clinical Data Associate I/II. This fully remote position in Bangalore offers the opportunity to work in a dynamic clinical research environment focused on ensuring data accuracy, integrity, and regulatory compliance. You’ll be an integral part of a team that supports end-to-end data cleaning and validation processes for global clinical trials involving investigational drugs and medical devices.


Key Responsibilities

  • Perform advanced data cleaning and validation activities for clinical studies

  • Identify and resolve data discrepancies in alignment with GCP, SOPs, and study guidelines

  • Update data management databases and track data clarifications and queries

  • Analyze data management reports and perform CRF design tasks if applicable

  • Review data listings for accuracy and consistency

  • Handle SAE (Serious Adverse Event) and third-party vendor data reconciliation

  • Generate regular status reports for internal teams and clients

  • Exercise independent judgment and initiative in solving complex data issues

  • Collaborate with global teams and communicate with cross-functional stakeholders


Required Skills & Qualifications

  • Strong understanding of Good Clinical Practices (GCP) and clinical data management processes

  • Hands-on experience in data discrepancy management and query resolution

  • Familiarity with clinical trial software and data management systems

  • Ability to manage SAE reconciliation and vendor data integration

  • Excellent attention to detail and problem-solving capabilities

  • Strong communication skills for collaboration and reporting

  • Prior experience in a CRO or clinical research setting preferred

  • Shift: Second Shift (Afternoons)

  • Environmental: Must comply with GMP safety standards


Perks & Benefits

  • Fully remote work setup

  • Work with a global leader in clinical research services

  • Collaborative and growth-focused environment

  • Involvement in cutting-edge clinical trials

  • Competitive salary (not specified, but industry-standard)

  • Opportunities for career advancement in a global organization


Company Description

As part of a top-tier Contract Research Organization (CRO), our clinical research team delivers world-class expertise in data management and drug development. We focus on accelerating the availability of safe and effective treatments across a wide range of therapeutic areas, powered by innovation and regulatory excellence.


Work Mode: Fully Remote
Location: Bangalore, Karnataka, India
Job Type: Full-time
Shift: Second Shift (Afternoons)


Call-to-Action

Ready to shape the future of clinical research? Apply now to become a key contributor as a Clinical Data Associate I/II. Help deliver data-driven insights that transform patient care globally.