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.

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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.

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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.

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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

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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.

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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.

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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.

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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.

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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.

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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.

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Eligibility Criteria

Educational Qualification

Candidates with the following qualifications are eligible:

• B.Pharm
• M.Pharm
• Pharm.D

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Experience Required

• 1 to 3 years of experience in:
  • Clinical Research
  • Clinical Trial Coordination
  • Healthcare Research Operations

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Knowledge Requirements

Candidates should have knowledge of:

• GCP Guidelines
• Clinical Trial Protocols
• Regulatory Documentation
• CRF Systems
• EDC Platforms

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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

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Soft Skills

Important professional skills include:

• Communication skills
• Organizational ability
• Attention to detail
• Team coordination
• Time management
• Documentation accuracy

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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

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Interview Details

Selection Process

The recruitment process may include:

1. Resume Shortlisting
2. HR Screening
3. Technical Clinical Research Interview
4. Final Discussion Round

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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

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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.

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How to Apply

Interested candidates can apply through the official job application link below:

Apply on Naukri.com

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

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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.

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2. What is the job location?

The job location is Vadodara, Gujarat.

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3. What qualifications are required for this role?

Candidates with B.Pharm, M.Pharm, or Pharm.D qualifications can apply.

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4. How much experience is required?

Candidates with 1–3 years of clinical research or clinical trial coordination experience are preferred.

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5. What are the important skills required?

Clinical trial coordination, CRF data entry, patient recruitment, GCP knowledge, and regulatory documentation skills are important.

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6. What is the estimated salary for this role?

The estimated salary range is approximately ₹3.5 LPA to ₹6.5 LPA.

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7. Is this a permanent job role?

Yes, this is a full-time permanent healthcare and clinical research role.

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8. Which industry does this role belong to?

The role belongs to the Healthcare & Life Sciences industry.

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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.

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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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