NEXVED RESEARCH Hiring Clinical Research Coordinator (CRC) in Chandigarh | Clinical Research Jobs 2026

(NEXVED RESEARCH Hiring Clinical Research Coordinator)

Introduction

The clinical research industry in India is continuously expanding with increasing opportunities for pharmacy, life sciences, and healthcare professionals. NEXVED RESEARCH has announced a new hiring opportunity for the position of Clinical Research Coordinator (CRC) in Chandigarh. This role is highly suitable for candidates with experience in clinical trial coordination, patient management, site documentation, and regulatory compliance.

Professionals looking for Clinical Research Coordinator jobs in Chandigarh, CRC jobs in India, clinical operations careers, and clinical trial site management opportunities should consider applying for this latest opening. Candidates with knowledge of ICH-GCP guidelines, clinical trial processes, and site coordination activities can significantly strengthen their careers through this opportunity.

Author: Pharmaduniya Editorial Team

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About NEXVED RESEARCH

NEXVED RESEARCH is a growing clinical research organization involved in supporting clinical trial operations, patient management, and regulatory-compliant research practices. The organization focuses on quality-driven clinical operations and efficient study site coordination while maintaining international clinical research standards.

The company works closely with investigators, sponsors, clinical teams, and research professionals to ensure smooth clinical trial execution and patient safety. NEXVED RESEARCH offers excellent exposure to clinical operations, trial coordination, regulatory documentation, and site management activities for healthcare and life sciences professionals.

Industry: Clinical Research & Healthcare Research
Company Type: Clinical Research Organization (CRO)
Location: Chandigarh, India
Work Focus: Clinical Operations, Site Coordination, Patient Management, Regulatory Compliance

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Job Overview Summary

NEXVED RESEARCH is hiring experienced Clinical Research Coordinators (CRC) for its Chandigarh clinical trial site. The selected candidates will support daily clinical trial activities, patient coordination, regulatory documentation, and site management operations.

The role requires strong coordination skills, understanding of clinical trial protocols, compliance with ICH-GCP guidelines, and the ability to manage multiple research activities effectively. Candidates will work closely with investigators, sponsors, monitors, and clinical teams to ensure the successful execution of clinical studies.

This CRC job provides valuable experience in clinical operations, regulatory processes, site coordination, and patient management within the growing clinical research industry.

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Vacancy Details

Particulars	Details
Job Role	Clinical Research Coordinator (CRC)
Company	NEXVED RESEARCH
Location	Chandigarh
Industry	Clinical Research
Employment Type	Full-Time
Experience Required	1–3 Years Preferred
Qualification	B.Pharm, M.Pharm, B.Sc, M.Sc Life Sciences
Department	Clinical Operations
Salary Estimate	₹3.0 LPA – ₹5.5 LPA
Application Mode	Email Application

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Clinical Research Coordinator Job Responsibilities Explained

Clinical Trial Coordination

The selected CRC will coordinate day-to-day clinical trial activities at the study site and ensure smooth execution of ongoing clinical research projects according to study protocols.

Investigator & CRA Support

Candidates will assist Principal Investigators and Clinical Research Associates (CRAs) with study-related operations, patient scheduling, documentation management, and regulatory compliance activities.

Patient Recruitment & Follow-Up

The role involves supporting patient recruitment, follow-up visits, coordination activities, and maintaining proper communication with trial participants throughout the study duration.

Documentation & Regulatory Compliance

Maintaining accurate study records, informed consent forms, regulatory files, and site documentation is one of the key responsibilities. The selected candidate must ensure compliance with ICH-GCP guidelines and SOP requirements.

Audit Readiness & Data Accuracy

Candidates will help maintain inspection readiness, ensure accurate study data, and support timely reporting for sponsors and internal clinical teams.

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Eligibility Criteria

Educational Qualification

Candidates should possess any of the following qualifications:

• B.Pharm
• M.Pharm
• B.Sc Life Sciences
• M.Sc Life Sciences
• Clinical Research qualification
• Other healthcare or science-related degrees

Experience Required

• 1–3 years of Clinical Research Coordinator (CRC) experience preferred
• Experience in:
  • Site coordination
  • Clinical trial documentation
  • Patient management
  • Regulatory compliance
  • Clinical operations

Preferred Knowledge

• ICH-GCP Guidelines
• Clinical trial processes
• SOP compliance
• Site management activities
• Regulatory documentation

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Skills Required

NEXVED RESEARCH is looking for candidates with strong operational and clinical research skills, including:

• Clinical trial coordination
• Patient management abilities
• Documentation and reporting skills
• Regulatory compliance understanding
• Strong communication skills
• Organizational abilities
• Attention to detail
• Team collaboration
• Time management
• Audit readiness support

Candidates with good interpersonal skills and the ability to manage multiple trial activities efficiently will have an advantage during the selection process.

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Salary Estimate

Based on current clinical research industry standards in India, the expected salary for the Clinical Research Coordinator role may range between:

₹3.0 LPA – ₹5.5 LPA

Actual compensation may vary depending on:

• Experience level
• Clinical trial exposure
• Site coordination knowledge
• Technical skills
• Interview performance

Additional benefits may include:

• Exposure to active clinical trials
• Career growth opportunities
• Regulatory compliance experience
• Site management exposure
• Clinical operations training

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Interview Details

Selection Process

The hiring process may include:

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

Topics Likely to be Assessed

Candidates may be evaluated on:

• ICH-GCP Guidelines
• Clinical trial coordination
• Site documentation
• Patient management
• Regulatory compliance
• SOP understanding
• Communication skills
• Clinical operations workflow

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Required Documents

Candidates applying for the NEXVED RESEARCH CRC position should keep the following documents ready:

• Updated Resume/CV
• Educational Certificates
• Experience Certificates
• Identity Proof
• Passport-size Photograph
• Internship Certificates (if available)
• Clinical Research Training Certificates
• Salary Slips (for experienced candidates)

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Why Join NEXVED RESEARCH?

Working with NEXVED RESEARCH allows candidates to gain practical experience in clinical trial execution, site management, patient coordination, and regulatory compliance activities.

Benefits of Joining

• Exposure to active clinical trials
• Experience in site operations
• Career growth in clinical research
• Opportunity to work with investigators and sponsors
• Strong learning environment
• Hands-on experience in regulatory documentation
• Development of clinical coordination skills

This opportunity is highly beneficial for candidates looking to build long-term careers in the CRO and clinical research industry.

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How to Apply

Interested and eligible candidates can share their updated CV via email:

📩 Email: info.nexvedresearch@gmail.com

Subject Line:
Application for Clinical Research Coordinator – Chandigarh

Candidates are advised to apply as early as possible since positions may close after suitable candidate selection.

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Frequently Asked Questions (FAQs)

Q1. What is the job role offered by NEXVED RESEARCH?

NEXVED RESEARCH is hiring for the position of Clinical Research Coordinator (CRC).

Q2. What qualifications are required for this CRC job?

Candidates with B.Pharm, M.Pharm, B.Sc, M.Sc Life Sciences, or related healthcare qualifications can apply.

Q3. What experience is preferred for this role?

Candidates with 1–3 years of Clinical Research Coordinator experience are preferred.

Q4. What is the location of this clinical research job?

The job location is Chandigarh, India.

Q5. What skills are important for this role?

Knowledge of ICH-GCP guidelines, documentation management, patient coordination, and clinical trial operations is important.

Q6. What is the expected salary for this CRC position?

The estimated salary range is approximately ₹3.0 LPA – ₹5.5 LPA.

Q7. How can candidates apply for this job?

Candidates can apply by sending their updated CV to info.nexvedresearch@gmail.com.

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Final Conclusion

NEXVED RESEARCH offers an excellent opportunity for clinical research professionals who want to strengthen their careers in clinical operations and site management. The Clinical Research Coordinator role provides valuable exposure to patient coordination, clinical trial execution, regulatory compliance, and documentation management.

Candidates interested in Clinical Research Coordinator jobs in Chandigarh, clinical operations careers, and CRO opportunities should consider applying for this role. With hands-on experience in active clinical studies and exposure to industry-standard research practices, this opportunity can significantly enhance long-term career growth in the clinical research industry.

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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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