Fresher Job Opportunity: Associate Trainee Clinical Data Coordinator at IQVIA

Are you a fresher or early-career professional eager to enter the fast-growing world of clinical research and data management? If you have strong attention to detail, good computer skills, and an interest in healthcare data, the Associate Trainee Clinical Data Coordinator role at IQVIA could be your perfect career launchpad. πŸš€

This role offers hands-on exposure to Clinical Data Management (CDM) processes and builds a strong foundation for long-term growth in the clinical research industry.


πŸ₯ About IQVIA

IQVIA is a globally respected organization operating at the intersection of clinical research, healthcare intelligence, and advanced analytics. The company partners with pharmaceutical, biotechnology, and medical device organizations to bring innovative treatments to patients worldwide.

With operations across multiple countries, IQVIA is known for its structured training programs, strong career paths, and exposure to international clinical research standardsβ€”making it an ideal workplace for freshers entering life sciences. 🌍


πŸ“Œ Job Role Overview

Associate Trainee Clinical Data Coordinator

This role focuses on accurate entry, processing, and maintenance of clinical trial data within Clinical Data Management Systems (CDMS). The position plays a crucial role in ensuring that clinical study data is reliable, well-organized, and compliant with standard procedures.

As a trainee, you will work under guidance while developing essential skills required for a successful career in clinical data management.


🧾 Key Responsibilities Explained

πŸ’» Clinical Data Entry & Processing

Your primary responsibility will be entering clinical data into designated systems with high accuracy and timeliness, as this data directly supports clinical trials and research outcomes.

Depending on project requirements, you may work in roles such as:

  • Data Entry Associate
  • File Room Associate
  • Scanning Associate
  • Indexing Associate

Assignments may vary based on project needs and manager direction.


πŸ“‚ Document Handling & Tracking

You will process, log, scan, and track clinical study documents following established guidelines. Proper document control ensures audit readiness and smooth data flow.


πŸ“Š Compliance with SOPs

You’ll be trained to understand and strictly follow Standard Operating Procedures (SOPs) and work instructions, ensuring compliance with clinical research and internal quality standards.


πŸ—‚οΈ Study File Maintenance

Assisting in maintaining clinical data management study files, ensuring documents are updated, correctly stored, and easily retrievable for project teams.


🀝 Team Collaboration

You’ll work closely with the Clinical Data Management (CDM) team, building professional relationships with colleagues, supervisors, and project stakeholders. Clear communication is key in this role.


πŸŽ“ Educational Qualifications

This position is highly suitable for freshers. Minimum requirements include:

  • High School Diploma or equivalent
  • An equivalent combination of education, training, or relevant experience may be considered

πŸ‘‰ No advanced degree is mandatory, making this role accessible to motivated entry-level candidates.


🧠 Skills & Competencies Required

To succeed in this role, candidates should have:

  • βœ… Strong attention to detail and accuracy
  • βœ… Good organizational and time-management skills
  • βœ… Basic to advanced computer proficiency
  • βœ… Clear written and verbal communication skills
  • βœ… Ability to work in a structured, process-driven environment
  • βœ… Strong teamwork and relationship-building abilities

These skills are essential for maintaining data quality and meeting project timelines.


πŸ“ˆ Career Growth for Freshers

This role acts as a gateway into the clinical research industry. With experience and strong performance, you can progress to roles such as:

  • Clinical Data Coordinator
  • Clinical Data Analyst
  • Senior CDM Associate
  • Clinical Project Support roles

IQVIA’s global exposure and learning-driven culture make it an excellent place to build a long-term career. 🌱


🌍 Why Choose IQVIA?

✨ Global exposure to clinical research projects
✨ Structured training and continuous learning
✨ Strong, process-driven work culture
✨ Stable career path in healthcare & life sciences
✨ Opportunity to contribute to improving patient outcomes worldwide


πŸ“ Final Thoughts

For freshers looking to enter the clinical research and healthcare data domain, the Associate Trainee Clinical Data Coordinator role at IQVIA is a smart and practical choice. It provides industry-relevant skills, exposure to global standards, and a strong professional foundation.

If you’re detail-oriented, eager to learn, and interested in healthcare innovation, this could be your first step toward a rewarding career. πŸ’Όβœ¨


πŸ”— Apply Now

πŸ‘‰ https://jobs.iqvia.com/en/jobs/R1527341-0


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