IQVIA Lab Project Coordinator Freshers Kochi
- IQVIA Hiring Lab Cent Project Coordinator 1 – Freshers Eligible | Kochi Hybrid Clinical Research Role
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Clinical Documentation & Regulatory Support
- Monitoring & Coordination Activities
- Process Improvement & Compliance
- Eligibility / Qualifications
- Educational Qualification
- Experience
- Skills Required
- Location & Salary
- Application Process
- Why This Role Matters in Healthcare
- Frequently Asked Questions (FAQs)
- 1. Who can apply for this role?
- 2. Is prior experience required?
- 3. What are the main responsibilities?
- 4. What is the career growth?
- 5. Is this a good entry-level pharma job?
- Summary Table
IQVIA Hiring Lab Cent Project Coordinator 1 – Freshers Eligible | Kochi Hybrid Clinical Research Role
IQVIA is hiring Lab Cent Project Coordinator 1 professionals for its clinical operations team in Kochi, India. This is a full-time hybrid opportunity designed for freshers and entry-level candidates looking to build a career in clinical research, centralized monitoring, and clinical trial operations. The role focuses on site tracking, regulatory documentation support, and laboratory coordination activities within global clinical studies.
Company Overview
IQVIA is a global leader in clinical research services, healthcare analytics, and life sciences consulting. The company partners with pharmaceutical, biotechnology, and healthcare organizations to accelerate drug development, optimize clinical trials, and improve patient outcomes worldwide.
With deep expertise in clinical operations, real-world evidence, and healthcare data, IQVIA enables faster and more efficient clinical trial execution. Working at IQVIA provides exposure to global clinical studies, regulatory workflows, and advanced clinical research systems.
Job Role & Responsibilities
As a Lab Cent Project Coordinator 1, you will support centralized monitoring activities, clinical documentation, and lab coordination tasks to ensure smooth execution of clinical trials.
Core Responsibilities
- Perform centralized monitoring activities for assigned clinical projects
- Update and maintain databases with participating site information
- Provide access and support for clinical systems such as Infosario Portal
- Ensure timely completion of assigned training modules and compliance tasks
Clinical Documentation & Regulatory Support
- Prepare and manage documentation required for regulatory dossiers
- Support kit shipment documentation including Kit Contents Chart (KCC), packing lists, and import permits
- Ensure documentation is audit-ready and aligned with regulatory standards
Monitoring & Coordination Activities
- Track and follow up on pending activities related to patient laboratory reports
- Coordinate with internal teams to ensure timely release of reports
- Support real-time monitoring activities and maintain data accuracy
Process Improvement & Compliance
- Participate in process improvement initiatives within clinical operations
- Ensure compliance with company SOPs, regulatory guidelines, and quality standards
- Maintain accurate records for audit readiness and inspection requirements
Eligibility / Qualifications
Educational Qualification
Candidates must have a minimum qualification in any discipline.
Required courses include:
B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), Biomedical Sciences, Clinical Research, Nursing, or any equivalent qualification
Experience
- Freshers are eligible to apply
- Prior internship or exposure to clinical research is an advantage
Skills Required
- Basic understanding of clinical research processes and documentation
- Strong analytical and problem-solving abilities
- Good communication and interpersonal skills
- Ability to manage multiple tasks and work under pressure
- Proficiency in MS Office tools (Word, Excel)
Location & Salary
- Job Location: Kochi, India
- Work Mode: Hybrid
- Employment Type: Full-time
- Salary: Competitive salary aligned with entry-level clinical research roles
Application Process
Interested candidates can apply through the official IQVIA careers portal:
Apply Here: https://jobs.iqvia.com/en/jobs/R1530127-0
Why This Role Matters in Healthcare
This role supports critical clinical trial operations by ensuring accurate documentation, timely monitoring, and efficient coordination between study teams. By contributing to smooth clinical workflows, this position helps accelerate drug development and improve patient outcomes globally.
Frequently Asked Questions (FAQs)
1. Who can apply for this role?
Freshers and candidates from Life Sciences, Pharmacy, or related backgrounds can apply.
2. Is prior experience required?
No. This is an entry-level role suitable for freshers.
3. What are the main responsibilities?
The role involves centralized monitoring, clinical documentation, and lab coordination tasks.
4. What is the career growth?
You can grow into Clinical Research Associate (CRA), Clinical Project Coordinator, or Clinical Operations roles.
5. Is this a good entry-level pharma job?
Yes. It is a strong starting point for a career in clinical research and healthcare analytics.
Summary Table
| Category | Details |
|---|---|
| Company | IQVIA |
| Vacancies | Lab Cent Project Coordinator 1 |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), Biomedical Sciences, Clinical Research, Nursing |
| Experience | Freshers Eligible |
To apply for this job please visit jobs.iqvia.com.
