IQVIA Hiring Freshers for Lab Central Project Coordinator 1 in Kochi for freshers. Entry-level clinical research job with global CRO experience. Apply now.
Looking to start your career in clinical research with a globally recognized organization? IQVIA is currently hiring for the position of Lab Central Project Coordinator I in Kochi, India. This entry-level role is ideal for fresh graduates or candidates with minimal experience who want to build a strong foundation in clinical operations and centralized monitoring. If you are detail-oriented and interested in working in a fast-paced clinical environment, this opportunity could be a great start.
Company Overview
IQVIA is a global leader in clinical research services, healthcare intelligence, and life sciences analytics. The organization supports pharmaceutical, biotech, and medical device companies by delivering data-driven insights that accelerate drug development and commercialization. With operations in multiple countries and a strong presence in India, IQVIA offers diverse career opportunities for professionals in clinical research, pharmacovigilance, data analytics, and regulatory domains.
Job Location & Employment Type
- Location: Kochi, Kerala, India
- Employment Type: Full-time
- Job Level: Entry-level / Fresher-friendly
Open Position / Department Details
- Job Title: Lab Central Project Coordinator I
- Department: Clinical Operations / Central Monitoring
- Industry: Clinical Research / CRO
This role focuses on centralized monitoring and coordination of laboratory-related clinical trial activities. The selected candidate will work closely with cross-functional teams to ensure smooth documentation and monitoring workflows.
Key Roles & Responsibilities
The Lab Central Project Coordinator will support centralized monitoring activities and assist in handling operational clinical trial tasks. Responsibilities include:
- Performing centralized monitoring tasks under minimal supervision for assigned projects.
- Completing all mandatory role-based training programs, including SOP acknowledgements and internal learning modules.
- Maintaining and updating active databases with site participation and project-related data.
- Providing access provisioning for internal clinical platforms such as portals used for lab coordination.
- Ensuring proper preparation and timely completion of regulatory documentation required for clinical kit shipment.
- Coordinating with internal teams to ensure patient laboratory reports are released on time.
- Tracking pending activities and following up with stakeholders for timely resolution.
- Maintaining complete documentation of monitoring activities for audit readiness and compliance.
- Participating in departmental initiatives aimed at improving clinical processes and workflows.
- Supporting cross-functional teams with documentation, compliance tracking, and operational coordination.
This role requires strong organizational abilities and the ability to multitask efficiently in a regulated clinical environment.
Eligibility Criteria
Education
- Minimum qualification: High School Diploma or equivalent
- Graduates in Life Sciences, Pharmacy, Biotechnology, or related fields may have an advantage
Experience
- 0 to 1 year of experience preferred
- Freshers with relevant academic exposure to clinical research or healthcare operations can apply
Skills Required
- Basic understanding of clinical systems and processes
- Strong attention to detail and documentation accuracy
- Ability to manage multiple tasks simultaneously
- Good analytical and problem-solving skills
- Excellent written and verbal communication in English
- Strong organizational and time management skills
- Proficiency in MS Word, Excel, and general computer applications
- Ability to work in a fast-paced and deadline-driven environment
- Team collaboration and interpersonal communication skills
Candidates who demonstrate adaptability and willingness to learn will be highly valued for this position.
Salary & Benefits
- Compensation: As per company norms
- Additional benefits may include corporate healthcare coverage, structured training programs, and career growth opportunities within a global CRO environment.
Selection Process
The recruitment process typically includes:
- Online application submission
- Resume screening by the recruitment team
- Virtual or telephonic interview rounds
- Final selection and offer release
Shortlisted candidates will be contacted directly by the company for further evaluation.
How to Apply
Candidates must apply through the official IQVIA careers portal. Applications are accepted via online mode only. Ensure that all details and credentials submitted during the application process are accurate and complete.
Important Dates
- Job Posted: Recently
- Last Date to Apply: February 25, 2026
Interested candidates are advised to apply as soon as possible due to the short application window.
Why Apply for This Pharma Job?
This opportunity is ideal for candidates aiming to enter the clinical research and CRO sector. IQVIA offers a structured corporate environment where freshers can gain exposure to real-world clinical trial operations. Working in centralized monitoring helps build strong skills in documentation, regulatory compliance, and cross-functional collaboration. The role also provides a pathway to advanced positions such as Clinical Trial Coordinator, Project Specialist, or Clinical Data Associate. If you are looking to begin your clinical research journey with a globally respected organization, this role offers both stability and long-term growth potential.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform that shares verified pharmaceutical and clinical research job updates for educational purposes. We are not a recruitment agency and are not affiliated with IQVIA or any hiring organization. Candidates are advised to apply only through the official company website and avoid sharing personal information with unauthorized sources.
Final Call-to-Action
If you are a fresher or entry-level candidate looking to start a career in clinical research, this IQVIA opportunity in Kochi is worth exploring. With global exposure, structured training, and strong career growth potential, this role can be your gateway into the clinical trials industry. Apply before the deadline and take the first step toward building a successful pharma career.
