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Clinical Trials Assistant - Job Opportunity at IQVIA

Singapore, Singapore
Full-time
Entry-level
Posted: January 17, 2025
Hybrid
SGD 36,000 - 48,000 per year based on Singapore market rates for entry-level clinical research positions

Benefits

Hybrid work arrangement offering flexibility
Professional development through clinical research exposure
Global company resources and training opportunities
Healthcare industry networking opportunities
Career advancement pathways in clinical research

Key Responsibilities

Support clinical documentation management and TMF maintenance with focus on regulatory compliance and data integrity
Coordinate clinical trial logistics including supplies tracking and documentation flow
Facilitate communication between clinical teams and maintain project documentation standards
Assist with site monitoring activities and quality control processes
Support data management and query resolution processes

Requirements

Education

Bachelors Degree in Pharmaceutical or related field

Experience

1 - 3 years of experience in clinical research environment

Required Skills

Good Clinical Practice (GCP) knowledge International Conference on Harmonization (ICH) guidelines familiarity Microsoft Word, Excel and PowerPoint proficiency Good written and verbal communication skills English language proficiency Time management and organizational skills Interpersonal relationship management
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Sauge AI Market Intelligence

Industry Trends

Increasing demand for clinical research support roles due to growing Asia-Pacific pharmaceutical market Rising complexity in clinical trial documentation requiring specialized assistants Shift towards electronic trial master file (eTMF) systems creating new skill requirements Growing importance of data integrity and regulatory compliance in clinical research

Role Significance

Typically works within a team of 5-8 people including CRAs and regulatory specialists
Entry to mid-level support role with significant responsibility for maintaining trial documentation integrity

Key Projects

Clinical trial documentation management Regulatory compliance support Site monitoring assistance Data quality control initiatives

Success Factors

Strong attention to detail and organizational skills Ability to maintain accurate documentation while meeting tight deadlines Effective communication with multiple stakeholders Understanding of clinical research processes and regulations

Market Demand

High demand with steady growth projected due to Singapore's position as a biomedical hub and increasing clinical trial activities in the region

Important Skills

Critical Skills

Documentation management expertise is fundamental for regulatory compliance GCP knowledge ensures adherence to international standards Communication skills crucial for stakeholder coordination Attention to detail essential for data accuracy

Beneficial Skills

Project management methodologies Electronic trial master file systems knowledge Therapeutic area expertise Quality management systems understanding

Unique Aspects

Opportunity to work with global clinical trials
Exposure to diverse therapeutic areas
Integration of technology in clinical trial processes
Strong professional development infrastructure

Career Growth

2-3 years in role before advancement opportunities, depending on performance and market conditions

Potential Next Roles

Clinical Research Associate (CRA) Clinical Trial Manager Regulatory Affairs Specialist Clinical Operations Coordinator

Company Overview

IQVIA

IQVIA is a global leader in clinical research and healthcare intelligence, formed from the merger of IMS Health and Quintiles

Top-tier position in clinical research services with significant market share and global presence
Strong Asia-Pacific presence with Singapore serving as a regional hub
Professional environment with emphasis on compliance, quality, and continuous learning
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