IQVIA is hiring for the role of Lab Project Services Coordinator in Kochi. This is a full-time clinical research job ideal for candidates looking to build a career in clinical trials, project coordination, and laboratory operations.
With increasing demand in the clinical research industry, this role offers exposure to study lifecycle management, centralized monitoring, and stakeholder coordinationโkey skills for long-term growth in CROs.
Job Overview
The Lab Project Services Coordinator supports project managers and study teams in executing clinical trials efficiently. The role spans across:
- Study start-up
- Ongoing monitoring
- Project close-out
Youโll work closely with clinical teams, investigators, and sponsors, ensuring compliance with SOPs and regulatory standards.
Key Responsibilities
Study Setup & Planning
- Assist in project meetings, prepare minutes & action logs
- Develop protocol-specific lab instruction documents
- Support centralized monitoring setup
Study Monitoring & Execution
- Manage site onboarding and investigator portal access
- Track kit shipments and lab logistics
- Monitor study performance and resolve queries
- Handle protocol deviations, escalations, and compliance issues
Data Monitoring & Reporting
- Analyze reports and identify performance trends
- Provide actionable feedback to stakeholders
- Support administrative and documentation tasks
Stakeholder Coordination
- Communicate with internal teams and external clients
- Handle responsibilities in absence of Project Manager
- Support audits, inspections, and training sessions
Qualifications & Eligibility
- Education:
- Bachelorโs Degree in Life Sciences (preferred)
- OR High School Diploma with relevant experience
- Experience:
- 0โ1+ years in clinical, medical, or healthcare domain
- Skills Required:
- Strong communication & coordination skills
- Critical thinking and problem-solving ability
- Time management and multitasking
- Proficiency in MS Office (Excel, Word, PowerPoint)
- Ability to work in fast-paced clinical environments
Salary & Benefits (Estimated)
- Salary Range: โน3.5 LPA โ โน6 LPA
- Exposure to global clinical trials
- Career growth in CRO & pharmacovigilance domains
- Training and development opportunities
- Work with international stakeholders
Why This Role Matters
This role is a strong entry point into:
- Clinical Project Management
- Clinical Data Management
- Pharmacovigilance & Safety Operations
If you’re targeting companies like IQVIA, Parexel, or Fortrea, this role builds core clinical operations experience.
How to Apply
