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Health Care Global Enterprises Hiring Clinical Research Coordinator in Vadodara | Clinical Research Jobs 2026
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Health Care Global Enterprises Hiring Clinical Research Coordinator in Vadodara | Clinical Research Jobs 2026
(Health Care Global Enterprises Hiring Clinical Research Coordinator in Vadodara)
Introduction
Health Care Global Enterprises is hiring for the position of Clinical Research Coordinator in Vadodara, Gujarat. This opportunity is highly suitable for candidates who want to build a long-term career in clinical research, healthcare operations, and clinical trial management.
Candidates with qualifications such as B.Pharm, M.Pharm, or Pharm.D and experience in clinical trial coordination, patient management, regulatory documentation, and CRF data handling are encouraged to apply for this healthcare and life sciences job opening.
The pharmaceutical and clinical research industry in India is expanding rapidly in 2026, increasing demand for professionals with knowledge of GCP guidelines, clinical protocols, EDC systems, and regulatory compliance. This role provides valuable exposure to clinical study operations and patient-focused healthcare environments.
About The Company
Health Care Global Enterprises Ltd., commonly known as HCG, is one of India’s leading healthcare organizations specializing in cancer care, oncology services, advanced diagnostics, and clinical research support.
The company is recognized for its patient-centered healthcare model and advanced treatment infrastructure across multiple cities in India. HCG focuses on high-quality medical care, clinical excellence, and healthcare innovation while supporting research-driven medical services.
Company Details
Company Name: Health Care Global Enterprises Ltd.
Industry: Healthcare & Oncology Services
Headquarters: Bengaluru, Karnataka, India
Founded: 1989
Employee Strength: 5,000+ Employees
Business Presence: Multiple Cancer Care Centers Across India
Work Model: Full-time Healthcare Operations
The organization provides opportunities for professionals interested in clinical research, healthcare management, oncology studies, and patient-focused medical operations.
Job Overview Summary
Health Care Global Enterprises is looking for an experienced Clinical Research Coordinator to manage and support clinical research activities at its Vadodara location.
The selected candidate will coordinate clinical trials, maintain regulatory documentation, support patient recruitment, handle CRF and EDC data entry, and ensure compliance with clinical research guidelines.
This role is ideal for candidates who want practical exposure to:
Clinical trial management
Clinical data handling
GCP compliance
Patient coordination
Regulatory documentation
Healthcare research operations
The position offers a strong learning environment and long-term growth opportunities in the clinical research and healthcare sector.
Vacancy Details
Job Details
Information
Company Name
Health Care Global Enterprises
Job Role
Clinical Research Coordinator
Job Location
Vadodara, Gujarat
Job Type
Full-Time, Permanent
Department
Healthcare & Life Sciences
Industry
Medical Services / Hospital
Qualification
B.Pharm, M.Pharm, Pharm.D
Experience Required
1–3 Years
Responsibility Explanation
1. Study Management
The selected candidate will oversee day-to-day clinical trial activities and ensure proper study coordination.
Key Activities:
Managing multiple clinical studies
Maintaining study documentation
Updating regulatory binders
Ensuring protocol compliance
Supporting study timelines
Proper study management helps maintain clinical trial quality and operational efficiency.
2. Participant Management
Clinical Research Coordinators play an important role in patient interaction and participant safety.
Major Responsibilities:
Identifying eligible study participants
Conducting informed consent procedures
Coordinating patient visits
Monitoring participant safety
Maintaining communication with patients
This responsibility ensures the ethical and smooth execution of clinical studies.
3. Clinical Procedures
The role also includes protocol-specific clinical support activities.
Responsibilities Include:
Recording vital signs
ECG monitoring
Blood sample collection
Laboratory sample processing
Supporting protocol procedures
These activities are important for collecting accurate clinical research data.
4. Data Management
Clinical data accuracy is highly important in research operations.
Key Responsibilities:
CRF data entry
EDC system updates
Query resolution
Source document maintenance
Data verification activities
Strong data management helps maintain research integrity and regulatory compliance.
5. Regulatory Compliance
The selected professional will support ethics submissions and regulatory documentation activities.
Responsibilities:
Preparing ethics committee submissions
Updating study-related documents
Ensuring GCP compliance
Maintaining regulatory records
Compliance activities are essential for smooth clinical trial operations.
6. Coordination & Communication
The role requires coordination with multiple stakeholders involved in clinical research studies.
Coordination Activities:
Working with Principal Investigators (PIs)
Communicating with sponsors and CROs
Supporting monitoring visits
Assisting with audit readiness activities
Good communication and teamwork skills are important for this role.
Eligibility Criteria
Educational Qualification
Candidates with the following qualifications are eligible:
B.Pharm
M.Pharm
Pharm.D
Experience Required
1 to 3 years of experience in:
Clinical Research
Clinical Trial Coordination
Healthcare Research Operations
Knowledge Requirements
Candidates should have knowledge of:
GCP Guidelines
Clinical Trial Protocols
Regulatory Documentation
CRF Systems
EDC Platforms
Skills Required
Technical Skills
Candidates should possess:
Clinical trial coordination knowledge
Patient recruitment understanding
CRF and EDC data entry skills
Regulatory documentation handling
Monitoring visit coordination
ECG and sample collection knowledge
Soft Skills
Important professional skills include:
Communication skills
Organizational ability
Attention to detail
Team coordination
Time management
Documentation accuracy
Salary Estimate
The estimated salary for this Clinical Research Coordinator role may range between ₹3.5 LPA to ₹6.5 LPA, depending on:
Experience level
Clinical trial exposure
Healthcare operations knowledge
Technical and regulatory expertise
Additional benefits may include:
Professional healthcare work environment
Clinical research exposure
Learning opportunities
Career growth in healthcare and CRO sectors
Stable full-time employment
Interview Details
Selection Process
The recruitment process may include:
Resume Shortlisting
HR Screening
Technical Clinical Research Interview
Final Discussion Round
Important Interview Topics
Candidates should prepare:
GCP Guidelines
Clinical trial process
CRF & EDC concepts
Patient recruitment process
Informed consent procedures
Regulatory documentation
Monitoring visit basics
Required Documents
Candidates should keep the following documents ready:
Updated Resume/CV
Educational Certificates
Experience Certificates
Government ID Proof
Passport-size Photograph
Internship or Training Documents
Clinical Research Certifications (if available)
Current Salary Details (if applicable)
Proper document organization may improve interview processing efficiency.
How to Apply
Interested candidates can apply through the official job application link below:
Candidates are advised to apply early and prepare a professional clinical research resume highlighting:
Trial coordination experience
GCP knowledge
CRF & EDC skills
Regulatory documentation exposure
Frequently Asked Questions (FAQs)
1. Which company is hiring for this clinical research role?
Health Care Global Enterprises is hiring for the Clinical Research Coordinator position.
2. What is the job location?
The job location is Vadodara, Gujarat.
3. What qualifications are required for this role?
Candidates with B.Pharm, M.Pharm, or Pharm.D qualifications can apply.
4. How much experience is required?
Candidates with 1–3 years of clinical research or clinical trial coordination experience are preferred.
5. What are the important skills required?
Clinical trial coordination, CRF data entry, patient recruitment, GCP knowledge, and regulatory documentation skills are important.
6. What is the estimated salary for this role?
The estimated salary range is approximately ₹3.5 LPA to ₹6.5 LPA.
7. Is this a permanent job role?
Yes, this is a full-time permanent healthcare and clinical research role.
8. Which industry does this role belong to?
The role belongs to the Healthcare & Life Sciences industry.
Final Conclusion
Health Care Global Enterprises offers an excellent opportunity for clinical research professionals looking to build long-term careers in healthcare research and clinical trial operations.
The Clinical Research Coordinator role provides practical exposure to:
Clinical study management
Patient coordination
Regulatory compliance
Clinical documentation
Healthcare research systems
As India’s clinical research and healthcare sector continues expanding in 2026, professionals with knowledge of GCP, CRF systems, EDC platforms, and patient-focused research operations are expected to remain in high demand.
Candidates interested in clinical research careers should consider applying early for this opportunity and prepare thoroughly for clinical research interviews and healthcare documentation processes.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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