IQVIA hiring Clinical Research Coordinators across India for experienced healthcare professionals seeking rewarding clinical research careers.
Short Description
IQVIA has announced recruitment for the position of Clinical Research Coordinator (CRC) across Noida, Kochi, and Thane locations. Candidates holding Bachelor’s or Master’s degrees in Pharmacy, Life Sciences, Biotechnology, Nursing, or related healthcare disciplines with 6 months to 3 years of clinical research experience are eligible to apply. This opportunity allows professionals to work with one of the world’s leading clinical research and healthcare organizations while contributing to innovative clinical trials and patient-focused research projects. IQVIA offers excellent learning opportunities, career advancement, and exposure to global clinical development programs. Interested candidates can submit their updated resumes through email application mode.
Introduction
Clinical research continues to play a vital role in advancing healthcare, developing innovative therapies, and improving patient outcomes worldwide. As pharmaceutical, biotechnology, and healthcare organizations increase their investments in research and development, the demand for skilled Clinical Research Coordinators is growing rapidly across India.
IQVIA, a global leader in healthcare analytics, technology solutions, and clinical research services, has announced recruitment for Clinical Research Coordinator positions at its Noida, Kochi, and Thane locations. The company is seeking motivated professionals with clinical research experience who can support study execution, site coordination, regulatory compliance, and patient management activities.
This opportunity is ideal for candidates who want to strengthen their careers in clinical research while working with one of the most respected organizations in the healthcare industry. The role provides exposure to clinical trial management, Good Clinical Practice (GCP), regulatory documentation, and collaboration with investigators, sponsors, and healthcare professionals.
Candidates searching for Clinical Research Jobs, Clinical Research Coordinator Jobs, B.Pharm Jobs, M.Pharm Jobs, Life Sciences Jobs, Biotechnology Careers, and Pharma Careers India should consider this excellent opportunity with IQVIA.
About Company
IQVIA is a globally recognized healthcare and life sciences organization that provides advanced analytics, technology solutions, and clinical research services to pharmaceutical, biotechnology, healthcare, and medical device companies worldwide. The company was formed through the merger of IMS Health and Quintiles, creating one of the largest and most influential organizations in the global healthcare sector.
Operating in more than 100 countries, IQVIA supports healthcare innovation by helping organizations accelerate drug development, improve clinical trial efficiency, and enhance patient outcomes. The company leverages data science, artificial intelligence, advanced analytics, and healthcare expertise to solve complex challenges across the healthcare ecosystem.
IQVIA’s services span clinical research, real-world evidence generation, healthcare consulting, regulatory support, market access solutions, and technology-enabled healthcare services. The organization collaborates with pharmaceutical companies, biotechnology firms, healthcare providers, and regulatory agencies to bring innovative therapies to patients faster.
The company is widely recognized for its commitment to scientific excellence, ethical research practices, and continuous innovation. Employees benefit from exposure to global projects, advanced technologies, and extensive professional development opportunities.
For professionals interested in Clinical Research Jobs, Regulatory Affairs Jobs, Pharmacovigilance Careers, Pharmaceutical Jobs, and Healthcare Research Opportunities, IQVIA offers an exceptional platform for career growth and international exposure.
Job Overview
| Particulars | Details |
|---|---|
| Company Name | IQVIA |
| Job Role | Clinical Research Coordinator (CRC) |
| Department | Clinical Research |
| Qualification | Bachelor’s or Master’s Degree in Pharmacy, Life Sciences, Biotechnology, Nursing, or Related Healthcare Disciplines |
| Experience | 6 Months – 3 Years |
| Job Location | Noida, Kochi, Thane |
| Employment Type | Full-Time / Fixed Term Contract |
| Salary | ₹3.0 – ₹6.5 LPA (Approx.) |
| Application Mode | Email Application |
| Selection Process | Resume Screening, Technical Evaluation, Interview |
Available Vacancies
Clinical Research Coordinator (CRC)
Locations
- Noida, Uttar Pradesh
- Kochi, Kerala
- Thane, Maharashtra
Experience Required
6 Months to 3 Years
Employment Type
Full-Time / Fixed Term Contract
Preferred Candidates
Immediate Joiners
Industry
Clinical Research, Healthcare and Life Sciences
Eligibility Criteria
Candidates interested in applying should meet the following requirements:
Educational Qualification
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
- Life Sciences Graduates
- Life Sciences Postgraduates
- Biotechnology Graduates
- Biotechnology Postgraduates
- Nursing Professionals
- Healthcare Discipline Graduates
Experience Requirement
- Minimum 6 months of clinical research experience.
- Maximum 3 years of relevant experience.
- Experience in clinical trial coordination preferred.
- Exposure to research documentation and compliance activities.
Additional Requirements
- Knowledge of clinical trial processes.
- Understanding of ICH-GCP guidelines.
- Strong communication abilities.
- Organizational and coordination skills.
- Ability to manage multiple responsibilities.
Required Skills
Technical Skills
- Clinical Trial Coordination
- Clinical Research Documentation
- Regulatory File Maintenance
- Data Collection and Reporting
- Study Site Coordination
- Patient Recruitment Support
- Protocol Compliance
- Clinical Database Management
- GCP Compliance
- Clinical Operations Support
Department Skills
- Clinical Research Processes
- ICH-GCP Guidelines
- Investigator Coordination
- Site Management Activities
- Essential Document Management
- Study Visit Coordination
- Clinical Trial Administration
- Research Compliance Monitoring
- Patient Follow-Up Activities
- Clinical Data Handling
Soft Skills
- Communication Skills
- Organizational Abilities
- Problem-Solving Skills
- Attention to Detail
- Team Collaboration
- Time Management
- Professional Conduct
- Adaptability
- Interpersonal Skills
- Multitasking Capability
Roles and Responsibilities
Selected candidates will be responsible for:
- Coordinating day-to-day clinical trial activities at study sites.
- Maintaining study documentation and regulatory records.
- Assisting investigators with patient recruitment activities.
- Scheduling patient visits and follow-up appointments.
- Ensuring compliance with GCP and ICH guidelines.
- Managing communication between investigators and sponsors.
- Maintaining accurate clinical trial records.
- Supporting clinical data collection and reporting activities.
- Tracking study timelines and project milestones.
- Monitoring protocol adherence throughout the study.
- Assisting with site management activities.
- Preparing and maintaining essential study documents.
- Supporting audit and inspection readiness activities.
- Coordinating research-related administrative functions.
- Ensuring quality and compliance standards are maintained.
Salary and Benefits
IQVIA offers competitive compensation packages along with extensive career development opportunities.
Expected Salary
- Estimated Salary Range: ₹3.0 LPA – ₹6.5 LPA
- Salary depends on qualifications, experience, and location.
Incentives
- Performance-based growth opportunities.
- Career progression programs.
- Learning and development initiatives.
Career Growth
Professionals may advance into:
- Senior Clinical Research Coordinator
- Clinical Research Associate (CRA)
- Site Management Associate
- Clinical Trial Specialist
- Clinical Operations Executive
- Clinical Project Coordinator
- Clinical Project Manager
Learning Opportunities
- Exposure to global clinical research projects.
- Hands-on experience in trial management.
- Advanced GCP and regulatory training.
- Cross-functional healthcare collaboration.
- Professional certification opportunities.
Employee Benefits
- Professional work environment.
- International exposure.
- Learning and development support.
- Career advancement pathways.
- Healthcare industry experience.
Selection Process
The recruitment process generally includes the following stages:
Resume Screening
Applications are reviewed based on qualifications, experience, and suitability.
Initial Assessment
Shortlisted candidates may undergo preliminary evaluation.
Technical Interview
Discussion regarding clinical research experience, GCP knowledge, and site coordination skills.
HR Interview
Assessment of communication skills, professional goals, and organizational fit.
Final Selection
Successful candidates receive further communication regarding onboarding and joining formalities.
Application Details
Email Application
Email ID
Documents Required
- Updated Resume/CV
- Educational Certificates
- Degree Certificates
- Experience Certificates
- Clinical Research Training Certificates
- Identity Proof
- Recent Photograph
Preferred Candidates
Immediate Joiners
Documents Required
Candidates should prepare the following documents before applying:
- Updated Curriculum Vitae
- Educational Qualification Certificates
- Academic Mark Sheets
- Degree Certificates
- Experience Letters
- Clinical Research Certifications
- GCP Training Certificates
- Government Identity Proof
- Passport Size Photographs
- Address Proof
- Professional References (Optional)
How to Apply
Step 1
Prepare an updated professional resume highlighting clinical research experience.
Step 2
Include details of study coordination, documentation, and GCP-related responsibilities.
Step 3
Collect all required supporting documents.
Step 4
Draft a professional email application.
Step 5
Attach your resume and supporting documents.
Step 6
Review all information carefully before submission.
Step 7
Send your application to the official recruitment email address.
Step 8
Monitor your email regularly for interview invitations and further communication.
Why Join This Company
IQVIA is considered one of the most prestigious organizations within the global healthcare and clinical research industry. Working with the company provides professionals access to large-scale clinical development programs, advanced research methodologies, and global healthcare projects.
Clinical Research Coordinators at IQVIA gain valuable experience managing clinical trials, coordinating study activities, maintaining regulatory compliance, and collaborating with healthcare professionals. Such exposure significantly strengthens professional expertise and creates opportunities for long-term career growth.
The company promotes a culture of innovation, continuous learning, and professional development. Employees have access to training programs, mentorship opportunities, and exposure to cutting-edge technologies used in modern clinical research.
IQVIA’s global presence allows professionals to work on diverse therapeutic areas and interact with multidisciplinary teams across different regions. This international exposure enhances technical capabilities and broadens career opportunities within the healthcare sector.
For individuals seeking Clinical Research Jobs, Pharmaceutical Jobs, Life Sciences Careers, Biotechnology Jobs, and Healthcare Research Opportunities, IQVIA offers an ideal platform to build a successful and rewarding professional journey.
Interview Preparation Tips
- Revise the fundamentals of clinical research.
- Study ICH-GCP guidelines thoroughly.
- Review clinical trial phases and processes.
- Prepare examples of site coordination activities.
- Understand patient recruitment procedures.
- Learn essential clinical research documentation requirements.
- Review protocol compliance concepts.
- Practice communication and coordination-related interview questions.
- Familiarize yourself with regulatory requirements.
- Research IQVIA and its services.
- Organize all documents before the interview.
- Demonstrate professionalism and attention to detail.
Conclusion
IQVIA’s Clinical Research Coordinator recruitment drive offers an excellent opportunity for professionals with 6 months to 3 years of experience to advance their careers in the rapidly growing clinical research industry. The positions available across Noida, Kochi, and Thane provide candidates with the opportunity to work with one of the world’s leading healthcare and life sciences organizations.
With competitive compensation, extensive learning opportunities, and exposure to global clinical research projects, this role is well-suited for pharmacy, biotechnology, life sciences, and healthcare professionals seeking long-term career growth. Candidates interested in Clinical Research Jobs, Clinical Trial Management Careers, Pharmaceutical Jobs, and Healthcare Research Opportunities should apply as early as possible to maximize their chances of selection.
Frequently Asked Questions (FAQs)
1. Which company is hiring Clinical Research Coordinators?
IQVIA is hiring Clinical Research Coordinators.
2. What is the experience requirement?
Candidates with 6 months to 3 years of experience can apply.
3. What qualifications are eligible?
Pharmacy, Life Sciences, Biotechnology, Nursing, and related healthcare graduates and postgraduates are eligible.
4. What are the job locations?
Noida, Kochi, and Thane.
5. What is the estimated salary range?
Approximately ₹3.0 LPA to ₹6.5 LPA.
6. Is prior clinical research experience required?
Yes, candidates should have 6 months to 3 years of relevant experience.
7. What is the application mode?
Applications are accepted via email.
8. Who is preferred for this position?
Immediate joiners are preferred.
9. What are the key responsibilities?
Clinical trial coordination, documentation management, patient scheduling, and compliance activities.
10. Is this a full-time opportunity?
Yes, it is a full-time or fixed-term contract position.
