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Associate Trainee, Clinical Data Coordinator

IQVIA
Fresher years
INR 3.5 LPA – 4.8 LPA
Kochi, India
2 June 29, 2026
Job Description
Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Associate Trainee, Clinical Data Coordinator

Company: IQVIA
Location: Kochi, India
Department: Clinical Data Management (CDM)
Job Type: Full-Time
Work Mode: Hybrid

JOB OVERVIEW

The Associate Trainee, Clinical Data Coordinator is responsible for supporting Clinical Data Management (CDM) activities by accurately processing, tracking, and entering clinical trial data into Clinical Data Management Systems (CDMS). The role involves clinical data entry, document processing, file management, indexing, scanning, quality checks, and maintaining study documentation to ensure accurate, timely, and compliant clinical trial data management.

KEY RESPONSIBILITIES

Clinical Data Entry

  • Enter clinical trial data into Clinical Data Management Systems (CDMS).

  • Process Case Report Form (CRF) data accurately.

  • Ensure timely and accurate clinical data entry.

  • Verify data completeness and consistency.

  • Maintain high data quality standards.

Clinical Document Management

  • Process and manage clinical study documents.

  • Track Case Report Forms (CRFs) and study documentation.

  • Perform document scanning and indexing activities.

  • Maintain organized study files and records.

  • Ensure proper document filing and retrieval.

Study File Administration

  • Support maintenance of Clinical Data Management study files.

  • Organize study documentation according to project requirements.

  • Maintain accurate document logs and tracking records.

  • Assist with file room and archival activities.

  • Ensure inspection-ready documentation.

Quality & Compliance

  • Follow CRF Tracking and Data Entry Guidelines.

  • Adhere to Standard Operating Procedures (SOPs) and work instructions.

  • Ensure compliance with Clinical Data Management processes.

  • Perform quality checks on entered data and documents.

  • Maintain confidentiality of clinical trial information.

Team Collaboration

  • Collaborate with Clinical Data Management team members.

  • Communicate effectively with project teams.

  • Support assigned operational activities.

  • Meet project timelines and productivity targets.

  • Build effective working relationships with colleagues and managers.

EDUCATIONAL QUALIFICATIONS

Required

Bachelor's Degree in:

  • Pharmacy (B.Pharm / M.Pharm)

  • Life Sciences

  • Biotechnology

  • Biochemistry

  • Microbiology

  • Biomedical Sciences

  • Zoology

  • Botany

  • Or a related Life Sciences discipline

Recent graduates / Freshers are encouraged to apply.

EXPERIENCE REQUIREMENTS

Required

  • Freshers or recent graduates.

  • No prior experience required.

Preferred

  • Internship or academic exposure to Clinical Research or Clinical Data Management.

  • Basic understanding of Clinical Trials.

  • Familiarity with Microsoft Office applications.

  • Knowledge of Good Clinical Practice (GCP) is an advantage.