Future of Clinical Research in India (Future of Clinical Research in India) Introduction India is rapidly becoming one of the world’s most important destinations for clinical research and clinical trial operations. With the expansion of the pharmaceutical industry, biotechnology sector, medical device innovations, and healthcare technology, the demand for skilled clinical research professionals is increasing significantly in 2026. The Indian clinical research industry is witnessing strong growth due to increasing global clinical trials, cost-effective research capabilities, a large patient population, skilled healthcare professionals, and improving regulatory frameworks. Major pharmaceutical companies, CROs (Contract Research Organizations), biotechnology firms, and healthcare startups are heavily investing in clinical trials and drug development activities across India. Today, clinical research is not limited to traditional clinical trial monitoring. The industry now include...
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NEXVED RESEARCH Hiring Clinical Research Coordinator (CRC) in Chandigarh | Clinical Research Jobs 2026
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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
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
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.
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
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.
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
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.
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
Interview Details
Selection Process
The hiring process may include:
Resume Shortlisting
HR Screening
Technical Interview
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
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)
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.
How to Apply
Interested and eligible candidates can share their updated CV via email:
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.
Disclaimer
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