IQVIA Hiring Associate Trainee Clinical Data Coordinator in Kochi

Pharma Hiring Hub; Ernakulam; On-site; INR 300,000 - 420,000; Full time

Benefits offered by this job

Structured onboarding

Technical training

Hybrid work

Global exposure

Professional development

Job summary

IQVIA in Kochi, Kerala invites fresh graduates for Associate Trainee – Clinical Data Coordinator. The hybrid role offers training in clinical data management, clinical research, and trial operations while working with global pharma clients.

The program supports B.Pharm, M.Pharm, BSc, MSc in Life Sciences or Biotechnology. It provides onboarding, practical exposure, and long-term career growth in healthcare data management with opportunities for progression.

Qualifications

• Fresh graduates with strong academic background in life sciences.
• Interest in clinical research and data management.
• Willingness to learn through structured training.

Responsibilities

• Perform clinical data entry into CDMS.
• Process, log, and maintain Case Report Forms (CRFs).
• Support file room, scanning, indexing, and document management activities.
• Maintain electronic and physical study documentation.
• Track study documents according to SOPs and GCP guidelines.
• Coordinate with Clinical Data Managers and project teams.
• Ensure data quality through careful review and verification.
• Complete assigned activities within project timelines.

Skills

CDM fundamentals

Excel & Word

Organizational skills

Analytical thinking

Time management

Team collaboration

GCP guidelines

Education

B.Pharm

M.Pharm

B.Sc Life Sciences

M.Sc Life Sciences

Biotechnology

Microbiology

Genetics

Biomedical Science

Other related Life Science disciplines

Job description

Clinical Data Management (CDM) has become one of the fastest-growing career options for pharmacy and life sciences graduates. Every clinical trial generates thousands of data points that must be collected, verified, reviewed, and maintained with complete accuracy before a medicine reaches patients. This responsibility is handled by Clinical Data Management professionals, making them an essential part of the drug development process.

IQVIA, one of the world’s leading healthcare intelligence and Contract Research Organizations (CROs), has announced an excellent career opportunity for fresh graduates by opening applications for the position of Associate Trainee – Clinical Data Coordinator at its Kochi office. This hybrid role is ideal for candidates who want to begin their careers in Clinical Data Management, Clinical Research, and Clinical Trial Operations while working with global pharmaceutical companies.

Whether you are a recent B.Pharm, M.Pharm, B.Sc, M.Sc, Biotechnology, or Life Sciences graduate, this opportunity provides structured training, practical exposure, and long-term career growth in one of the most promising healthcare sectors.

Job Overview

Particulars

Details

Company IQVIA

Position Associate Trainee – Clinical Data Coordinator

Location Kochi, Kerala (Hybrid)

Employment Type Full-Time

Experience Freshers / Recent Graduates

Qualification B.Pharm, M.Pharm, B.Sc, M.Sc, Biotechnology & Life Sciences

Reference Code R1554381

Last Date 30 June 2026

About IQVIA

IQVIA is a globally recognized healthcare intelligence company that combines clinical research, advanced analytics, and healthcare technology to support pharmaceutical, biotechnology, and medical device organizations. With operations in more than 100 countries, IQVIA plays a significant role in accelerating clinical research while improving patient outcomes through high-quality data management and scientific innovation.

Working at IQVIA gives fresh graduates an opportunity to learn global clinical trial processes, international quality standards, and advanced Clinical Data Management systems used by leading pharmaceutical companies.

What Will You Do as a Clinical Data Coordinator?

As an Associate Trainee, you will work with experienced Clinical Data Management professionals to ensure that clinical trial information is collected, processed, and maintained accurately. Your work will directly contribute to maintaining the integrity of clinical research data before regulatory submissions and database lock activities.

• Perform clinical data entry into Clinical Data Management Systems (CDMS).
• Process, log, and maintain Case Report Forms (CRFs).
• Support file room, scanning, indexing, and document management activities.
• Maintain electronic and physical study documentation.
• Track study documents according to SOPs and GCP guidelines.
• Coordinate with Clinical Data Managers and project teams.
• Ensure data quality through careful review and verification.
• Complete assigned activities within project timelines.

Eligibility Criteria

IQVIA is looking for recent graduates who have a strong academic background and an interest in clinical research and healthcare data management.

• B.Pharm
• M.Pharm
• B.Sc Life Sciences
• M.Sc Life Sciences
• Biotechnology
• Microbiology
• Genetics
• Biomedical Science
• Other related Life Science disciplines

Skills That Can Help You Succeed

• Clinical Data Management fundamentals.
• Basic Microsoft Excel and Word knowledge.
• Organizational abilities.
• Analytical thinking.
• Time management.
• Team collaboration.
• Understanding of GCP guidelines.

Salary & Benefits

Apart from competitive compensation, selected candidates can expect structured onboarding, technical training, exposure to global clinical studies, hybrid work flexibility, and opportunities for continuous professional development within IQVIA’s Clinical Data Management teams.

Clinical Data Management offers excellent long-term career opportunities. After gaining experience, professionals can progress into positions such as Clinical Data Coordinator, Clinical Data Associate, Clinical Data Manager, Lead Data Manager, Clinical Project Manager, and Clinical Operations Manager. Professionals with expertise in data standards, EDC systems, and database programming are in particularly high demand across global CROs and pharmaceutical companies.