Location: Thane, Maharashtra, India
Job Type: Full-Time
Company: IQVIA
Job Requisition ID: R1534441
Application Deadline: May 1, 2026
Experience Required: 6–9 years (Not suitable for freshers)
About the Company
IQVIA is a global leader in clinical research services, healthcare analytics, and commercial insights. The organization plays a pivotal role in accelerating drug development and improving patient outcomes through advanced data-driven solutions and innovative clinical strategies.
Job Overview
The Manager – Lab Central Monitoring is responsible for leading and managing a team of Centralized Monitoring Project Coordinators (CPCs). This role focuses on ensuring operational excellence, maintaining data quality standards, and driving productivity across global clinical studies. The position requires strong leadership, regulatory knowledge, and cross-functional collaboration within clinical research environments.
Key Responsibilities
Lead, manage, and mentor a team of Centralized Monitoring Project Coordinators (CPCs) to ensure efficient execution of assigned activities
Plan, assign, and oversee daily operations while supporting training, performance evaluation, and professional development
Handle employee engagement, performance management, and resolution of workplace issues in line with organizational policies
Collaborate with global project teams and operational stakeholders to ensure consistent quality and delivery across studies
Participate in recruitment, candidate evaluation, onboarding, and training of new team members
Ensure team readiness by providing access to required systems, tools, SOPs, and structured training programs
Allocate resources effectively based on project needs, employee expertise, and workload distribution
Monitor team performance through regular audits, quality checks, and reporting of key metrics
Lead investigations into quality issues, perform root cause analysis, and implement CAPA (Corrective and Preventive Actions)
Identify operational risks and proactively implement mitigation strategies
Drive continuous improvement initiatives to enhance service delivery and maintain high-quality standards
Required Qualifications and Skills
Minimum High School Diploma or equivalent (Life Sciences or related background preferred)
6–9 years of experience in clinical research, centralized monitoring, or related domains
3–5 years of experience in team management or line management roles
Strong understanding of clinical research regulations including ICH-GCP guidelines
Basic knowledge of therapeutic areas and clinical trial protocols
Excellent communication, leadership, and stakeholder management skills
Strong organizational, problem-solving, and time management capabilities
Proficiency in MS Office and clinical systems with strong analytical skills
Ability to manage multiple priorities in a fast-paced, global work environment
Why This Role Matters
Opportunity to lead global clinical monitoring operations within a top-tier CRO
Exposure to international clinical trials and cross-functional collaboration
Strategic leadership role influencing data quality and patient safety
Career growth in clinical operations, centralized monitoring, and leadership pathways
Important Note for Applicants
This is a mid-to-senior level leadership role requiring prior experience in clinical research and team management. Freshers are advised to begin with entry-level roles such as Clinical Research Coordinator (CRC), Clinical Data Associate, or Pharmacovigilance Associate before progressing to managerial positions.
About Hiring Integrity
IQVIA maintains strict integrity standards in its hiring process. Any false information, misrepresentation, or omission during recruitment may result in disqualification or termination in accordance with applicable regulations.
How to Apply
Apply through the official careers page of IQVIA or explore verified global clinical research opportunities on ThePharmaDaily.com to accelerate your career in the pharmaceutical and clinical research industry.
Uttar Pradesh :
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