PHARMAFull-time
Assoc Lab Project Svcs Mgr
By Admin · Research & Development (Lab & Science)
BANGALORE (IN)ONSITEPOSTED: 8/19/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
ROLE DEFINITION & RESPONSIBILITIES
Core Responsibilities & Study Lifecycle Management
Manage end-to-end central laboratory operations and deliverables for assigned Phase I-IV clinical trial programs across study start-up, maintenance, and closeout phases.
Act as the primary operational point of contact for global pharmaceutical sponsors and clients following study award.
Review study protocols and budgets, lead kick-off meetings, develop Project Management Plans (PMP), and maintain milestone tracking, risk logs, and issue escalation registers.
Collaborate closely with the Study Setup team to ensure high-quality laboratory database configuration, custom kit designs, and protocol-specific document preparation.
Operational Monitoring, Finance & eTMF
Track project timelines, monitor deliverable milestones, and oversee central laboratory data transfers and reporting.
Manage clinical study documentation throughout the project lifecycle, ensuring timely and compliant filing into the electronic Trial Master File (eTMF).
Oversee study scope management, budget tracking, and contract modifications while actively monitoring service quality and resolving operational discrepancies.
Participate in proposal preparations, business development bids, and sponsor bid defense presentations.
Stakeholder Engagement & Site Support
Deliver study-specific laboratory training to clinical investigator sites, Clinical Research Associates (CRAs), and sponsor project teams.
Present protocol-specific materials at global Investigator Meetings and support client quality audits and regulatory inspections.
Serve as the main operational escalation point, triaging site queries regarding sample collection kits, logistics, specimen storage, and laboratory alerts.
Work Schedule
Operates on an Evening shift schedule (starting 5:00 PM onwards) in an office-based environment.
REQUIRED VERIFIED SKILLS
Clinical Project Management
Central Laboratory Operations
Study Setup
Protocol Review
eTMF Filing
Clinical Trial Lifecycle
Budget & Scope Tracking
Risk & Issue Management
Phase I-IV Trials
Stakeholder Communication
COMPENSATION & REWARDS
₹7.0L - 12.0L per annum
ORGANIZATION CONTEXT & CULTURE
IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.
TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research
RECOMMENDED TRAINING
1/4
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