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CRA 2 (Clinical Research Associate II) - Job Opportunity at IQVIA

Thane, India
Full-time
Mid-level
Posted: April 17, 2025
Hybrid
INR 8,00,000 - 12,00,000 per annum based on location and experience level

Benefits

Comprehensive healthcare package typical for global CRO
Professional development and training programs
Global mobility opportunities
Industry-standard benefits package

Key Responsibilities

Lead site monitoring and quality assurance for clinical trials according to GCP/ICH guidelines
Drive and optimize subject recruitment strategies across assigned sites
Conduct comprehensive site training and maintain regulatory compliance
Manage site documentation and regulatory submissions
Collaborate with cross-functional teams for project execution
Oversee financial aspects of site management where applicable

Requirements

Education

Bachelor's Degree in scientific discipline or healthcare preferred

Experience

At least 1 year of on-site monitoring experience

Required Skills

Good Clinical Practice (GCP) knowledge ICH guidelines expertise Microsoft Office proficiency Written and verbal communication skills Organizational and problem-solving skills Time and financial management Relationship management abilities
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Industry Trends

Increased adoption of decentralized clinical trials is reshaping the CRA role, requiring enhanced digital competencies Growing focus on Asia-Pacific region for clinical trials is creating expanded opportunities for CRAs in India Rising complexity in trial protocols is elevating the importance of experienced monitoring professionals

Role Significance

Typically works within a team of 5-8 CRAs under a Clinical Research Manager
Mid-level position with significant responsibility for trial quality and compliance

Key Projects

Phase II-IV clinical trials Site management and monitoring activities Quality assurance and compliance projects Site staff training and development initiatives

Success Factors

Strong understanding of clinical research regulations and GCP guidelines Excellent site relationship management capabilities Efficient time management and organizational skills Ability to work independently while maintaining team collaboration Strong attention to detail and quality focus

Market Demand

High demand with steady growth projected due to increasing clinical trial activities in India and APAC region

Important Skills

Critical Skills

GCP/ICH knowledge for ensuring trial compliance and quality Site management skills for maintaining productive site relationships Technical understanding of clinical trial processes Communication skills for effective stakeholder management

Beneficial Skills

Experience with electronic data capture systems Knowledge of local regulatory requirements Project management capabilities Therapeutic area expertise

Unique Aspects

Role combines traditional monitoring with evolving digital trial management
Position at global leader provides exposure to diverse therapeutic areas
Opportunity to work on cutting-edge clinical research projects

Career Growth

2-3 years in current role before advancement opportunity

Potential Next Roles

Senior CRA Clinical Research Manager Clinical Operations Manager Project Manager

Company Overview

IQVIA

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry

Fortune 500 company with strong market presence and continued growth in clinical research services
Major player in India's clinical research market with significant expansion plans
Fast-paced, global environment with emphasis on quality and compliance
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