IQVIA Hiring Clinical Trials Assistant in Singapore 2025 | ₹26.80–₹40.20 Lakhs Salary | Hybrid Work

Apply for high-paying Clinical Trials Assistant jobs at IQVIA Singapore 2025. Earn SGD 40,000–60,000 annually (₹26.80–₹40.20 Lakhs). Full-time hybrid clinical research jobs with global exposure and career growth.

IQVIA Hiring Clinical Trials Assistant in Singapore 2025 | ₹26.80–₹40.20 Lakhs Salary | Hybrid Work

IQVIA, a world-leading provider of clinical research services and healthcare intelligence, is actively hiring Clinical Trials Assistants (CTA) for its rapidly expanding operations in Singapore. This hybrid role offers excellent global exposure, competitive salaries, and a clear career path in clinical research — making it one of the top opportunities for life sciences graduates and administrative professionals looking to enter the clinical trials industry.

With over 87,000 employees worldwide and operations in 100+ countries, IQVIA is driving healthcare innovation by providing critical support for pharmaceutical companies, biotech firms, and medical device manufacturers globally.

🌐 About IQVIA – Company Overview

• Location: Singapore (Hybrid work model; multiple locations globally)

• Global Workforce: 87,000+ professionals

• Industry Focus: Clinical Research, Healthcare Analytics, Real-World Evidence, Market Access

• Compliance: Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines

• Mission: Accelerating medical innovation and improving patient outcomes globally

• Official Website: jobs.iqvia.com

IQVIA integrates clinical research, healthcare intelligence, and data-driven technology solutions, helping pharma companies deliver breakthrough therapies faster while maintaining regulatory compliance.

📝 Clinical Trials Assistant (CTA) – Job Details

Exchange rate used: 1 SGD = ₹67

🔬 Key Responsibilities

As a Clinical Trials Assistant (CTA) at IQVIA, your primary responsibility is to support clinical research operations while ensuring the accuracy and compliance of clinical trial documentation.

• Document Management: Assist CRAs and RSU teams in maintaining accurate Trial Master File (TMF) documentation.

• Regulatory Support: Prepare, distribute, file, and archive clinical documentation following Good Clinical Practice (GCP) and ICH guidelines.

• Data Management: Manage Case Report Forms (CRFs), queries, and data tracking to ensure smooth clinical data flow.

• Clinical Supplies: Assist with inventory management and distribution of Clinical Trial Supplies (CTS).

• Communication: Serve as a central contact for project communications, team coordination, and sponsor updates.

• Monitoring Support: May accompany Clinical Research Associates (CRAs) on site visits after completing required training.

• Periodic Review: Conduct study file reviews for documentation completeness and regulatory readiness.

🎓 Job Requirements & Qualifications

Education:

• Bachelor’s degree in Pharmaceutical Sciences, Life Sciences, Healthcare, Biotechnology, or related fields.

Experience:

• 1–3 years in a clinical research or healthcare environment preferred.

• Strong administrative candidates with no direct clinical research experience are also encouraged to apply.

Core Competencies:

• Basic knowledge of GCP, ICH guidelines, and clinical research protocols (Training provided).

• Strong organizational, documentation, and time management skills.

• Excellent proficiency in Microsoft Office (Word, Excel, PowerPoint).

• Effective verbal and written communication skills, including professional business English.

• Ability to collaborate with cross-functional teams and maintain strong client relationships.

• Positive attitude, proactive work ethic, and eagerness to learn.

💰 Salary & Benefits Package

• Annual Salary: SGD 40,000 – 60,000 (Approx ₹26.80 – ₹40.20 Lakhs INR)

• Global Exposure: Opportunity to work with cross-border clinical teams, sponsors, and multinational trials.

• Career Growth: Comprehensive GCP training, exposure to Trial Master File (TMF) management, and future promotion to CRA or Regulatory roles.

• Hybrid Work Model: Work-from-home flexibility combined with office-based collaboration.

• Professional Development: Access to IQVIA Learning Programs and continuous skill-building opportunities.

🚀 Career Advancement Opportunities at IQVIA

IQVIA’s Clinical Trials Assistant role is a perfect launchpad for multiple career paths in clinical research:

• Clinical Research Associate (CRA)

• Regulatory and Start-Up Specialist (RSU)

• Clinical Project Manager (CPM)

• Trial Master File Specialist

• Data Manager

• Clinical Operations Lead

With global projects and access to IQVIA’s proprietary healthcare intelligence platforms, employees are equipped with tools and training to grow into senior leadership roles across clinical research, regulatory affairs, and clinical data management.

🌟 Why This Role Is Critical

This position directly supports IQVIA’s mission to optimize clinical trials by improving documentation accuracy, regulatory compliance, and operational efficiency.

• Singapore’s biopharma industry is rapidly expanding with over 2,000 new clinical research and biotech jobs forecasted in the next few years.

• IQVIA’s clinical trials in Singapore directly contribute to faster approval timelines for innovative medical treatments worldwide.

🏢 Work Environment & Culture

• Hybrid work model: Mix of remote work and onsite office collaboration.

• Access to advanced clinical systems, TMF software, and real-time project dashboards.

• Collaborative global teams with strong mentorship programs.

• Occasional site visits post-training to develop clinical monitoring skills.

🔐 Important Fraud Prevention Note

IQVIA never charges candidates any fees for application, recruitment, or onboarding. Always verify job openings through official channels.

• Apply only via: jobs.iqvia.com

• Report any suspicious emails or activities directly to IQVIA HR.

💡 Interview Preparation Tips

• Highlight any experience in administration, clinical research, documentation management, or healthcare data.

• Familiarize yourself with Good Clinical Practice (GCP) and Trial Master File (TMF) concepts.

• Prepare to answer:

  • “What do you understand about clinical trial documentation compliance?”

  • “How do you ensure timelines are met while handling complex clinical data?”

  • “What is your understanding of GCP guidelines?”

🌏 Why Singapore Is a Global Clinical Research Hub

• Singapore is recognized as Asia’s clinical research powerhouse.

• Over 2,000 active clinical research jobs in pharma, CROs, and biotech.

• Government support for R&D, advanced clinical facilities, and a strong regulatory framework.

• Multinational pharma companies and global CROs have major regional offices in Singapore.

🌟 Join IQVIA’s Global Mission

IQVIA is at the forefront of healthcare innovation, driving breakthroughs in clinical trials, data analytics, and real-world evidence. By joining IQVIA’s Singapore clinical operations team, you contribute directly to improving patient outcomes globally.

👉 Apply today and take your clinical research career to the next level with IQVIA Singapore!