Location: Kochi, India (On-site, 5 Days Working)
Company: IQVIA
Job Type: Full-Time
Application Deadline: May 1, 2026
Job ID: R1531493
About the Company
IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights for the life sciences industry. The organization leverages advanced analytics, technology, and domain expertise to accelerate the development and commercialization of innovative medical treatments, improving patient outcomes worldwide.
Job Overview
The Associate Manager – Centralized Monitoring is a leadership role responsible for managing and supporting a team of Centralized Monitoring Project Coordinators (CPCs). This position plays a critical role in ensuring high-quality delivery of centralized monitoring activities, maintaining compliance with global clinical research standards, and driving operational excellence across studies.
This role requires a strong clinical background, leadership capability, and hands-on experience in managing teams within hospital, laboratory, or clinical research environments.
Experience Required
5–8 years of relevant experience in clinical research, laboratory operations, or hospital-based roles
Minimum 1–2 years of direct people management or line management experience
Not suitable for freshers
Educational Qualification
Bachelor’s degree or higher in Life Sciences, Pharmacy, Nursing, or related clinical field
Key Responsibilities
Lead, manage, and mentor a team of Centralized Monitoring Project Coordinators (CPCs)
Plan, assign, and oversee centralized monitoring activities for clinical studies and non-protocol tasks
Drive performance management, employee development, and training initiatives
Handle employee relations, performance appraisals, and HR-related actions in alignment with company policies
Collaborate with global project teams and cross-functional stakeholders to ensure consistent quality and delivery standards
Participate in recruitment, onboarding, and training of new team members
Ensure team readiness by providing access to systems, SOP training, and ongoing mentorship
Allocate resources effectively across projects based on team expertise and workload
Conduct regular quality checks and mini audits to maintain data accuracy and compliance
Lead investigations for quality issues, perform root cause analysis, and implement CAPA plans
Identify operational risks and implement corrective and preventive strategies
Track team performance metrics and report insights to senior management
Contribute to continuous improvement initiatives to enhance service delivery and operational efficiency
Core Skills and Competencies
Strong knowledge of clinical research regulations including ICH-GCP guidelines
Understanding of clinical trial protocols, centralized monitoring, and data review processes
Excellent leadership, team management, and interpersonal skills
Strong analytical thinking, problem-solving, and decision-making abilities
Effective communication skills with high proficiency in English
Ability to manage multiple priorities and work in a fast-paced environment
Proficiency in MS Office and clinical systems
Why This Role Matters
This position is critical in ensuring data integrity, patient safety, and regulatory compliance across clinical trials. As a leadership role, it offers the opportunity to directly influence study quality, team performance, and global project outcomes within a high-impact clinical research environment.
Important Compliance Note
IQVIA follows a strict zero-tolerance policy for recruitment fraud. Candidates are required to provide accurate and complete information throughout the hiring process. Any discrepancies may lead to disqualification or termination in accordance with applicable regulations.
How to Apply
Apply through the official careers portal of IQVIA. For more verified and latest clinical research, pharmacovigilance, and healthcare job opportunities, visit ThePharmaDaily.com.
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