NovoBliss Research Hiring Project Coordinator in Ahmedabad | CRO & Clinical Research Jobs 2026
NovoBliss Research Hiring Project Coordinator in Ahmedabad – Apply for CRO & Clinical Research Jobs 2026
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(NovoBliss Research Hiring Project Coordinator in Ahmedabad) |
Introduction
NovoBliss Research has announced a new career opportunity for experienced professionals in Clinical Research and CRO Operations for the position of Project Coordinator at its Ahmedabad office in Gujarat. This latest clinical research job is ideal for candidates with experience in clinical study coordination, project management, regulatory compliance, and CRO workflow operations.
Professionals with backgrounds in Pharmacy, Life Sciences, Clinical Research, and Regulatory Coordination can apply for this full-time on-site role. Candidates with knowledge of GCP guidelines, CDSCO regulations, ISO standards, and clinical trial documentation processes will have an added advantage.
This Project Coordinator role provides excellent exposure to clinical trial operations, quality systems, study management, and stakeholder coordination in a regulated Contract Research Organization (CRO) environment.
Candidates interested in building long-term careers in Clinical Research, Clinical Operations, CRO Project Management, and Regulatory Compliance should not miss this opportunity.
About NovoBliss Research
Company Overview
NovoBliss Research Private Limited is a CDSCO-registered and ISO 9001:2015 certified Contract Research Organization (CRO) headquartered in Ahmedabad, Gujarat, India. The company specializes in clinical safety and efficacy studies across multiple sectors, including pharmaceuticals, nutraceuticals, cosmetics, OTC products, dental care, and personal healthcare products.
NovoBliss Research operates with strong ethical, scientific, and regulatory standards and is associated with recognized organizations such as:
- Indian Society for Clinical Research (ISCR)
- Advertising Standards Council of India (ASCI)
The company focuses on delivering quality-driven clinical research services and supports healthcare brands through scientifically validated clinical studies and regulatory-compliant operations.
NovoBliss Research provides professionals with opportunities to work in clinical trial management, project coordination, documentation systems, compliance operations, and quality-focused clinical research environments.
The company has developed a reputation for maintaining high operational standards in CRO services and regulatory compliance activities.
Job Overview Summary
NovoBliss Research is currently hiring for the role of Project Coordinator at its Ahmedabad office. This role is designed for professionals experienced in Clinical Research Operations, CRO workflow management, study coordination, and regulatory compliance activities.
The selected candidates will manage clinical study timelines, coordinate project deliverables, maintain study documentation, support stakeholder communication, and ensure adherence to GCP, CDSCO, and ISO compliance requirements.
This position offers valuable exposure to clinical trial management processes, regulatory systems, quality documentation, and operational coordination within a certified CRO environment.
Professionals interested in Clinical Project Management and CRO Operations can use this opportunity to strengthen their careers in the pharmaceutical and healthcare research industry.
Vacancy Details
| Particulars | Details |
|---|---|
| Job Role | Project Coordinator |
| Company | NovoBliss Research Private Limited |
| Location | Ahmedabad, Gujarat, India |
| Industry | Clinical Research / CRO |
| Job Type | Full-Time |
| Work Mode | On-site |
| Qualification | B.Pharm, M.Pharm, Life Sciences or Related Discipline |
| Experience | CRO / Clinical Research Experience Preferred |
Job Role Explanation
Project Coordinator – CRO Operations
The Project Coordinator plays a critical role in ensuring smooth execution of clinical research projects and study-related activities. Candidates selected for this role will coordinate clinical trial workflows, support documentation management, monitor project timelines, and maintain communication with stakeholders and research teams.
This role requires strong organizational skills, project management capabilities, and knowledge of clinical research regulations and quality systems. Professionals working in this position will also support operational planning, regulatory coordination, and study documentation processes.
The position is highly suitable for candidates looking to build careers in:
- Clinical Research
- Clinical Operations
- CRO Management
- Regulatory Affairs
- Clinical Trial Coordination
- Quality and Compliance Operations
Key Responsibilities
Selected candidates will handle multiple project coordination and operational activities within the CRO environment.
Major responsibilities include:
- Coordinating clinical research projects and study activities
- Managing project timelines and operational deliverables
- Ensuring compliance with GCP, CDSCO, and ISO standards
- Maintaining study documentation and project reports
- Communicating with sponsors, clients, and internal stakeholders
- Supporting workflow management across clinical operations
- Monitoring project progress and maintaining accurate records
- Assisting in quality assurance and regulatory activities
- Supporting documentation review and compliance processes
- Coordinating with cross-functional research teams
Candidates will also gain exposure to clinical trial documentation systems and regulated healthcare project operations.
Eligibility Criteria
Educational Qualification
Applicants should possess:
- B.Pharm
- M.Pharm
- Life Sciences Degree
- Or related healthcare/science discipline
Experience Required
- CRO project coordination experience preferred
- Clinical research operations experience preferred
- Experience in study coordination and documentation management will be beneficial.
Job Location
- Ahmedabad, Gujarat, India
Skills Required
Candidates applying for this Project Coordinator role should possess technical, communication, and operational coordination skills.
Preferred skills include:
- Knowledge of GCP guidelines
- Understanding of CDSCO regulations
- Familiarity with ISO 9001:2015 standards
- Clinical trial coordination knowledge
- Project management and workflow coordination
- Strong documentation management skills
- Communication and stakeholder management abilities
- MS Office proficiency
- Ability to manage multiple projects simultaneously
- Regulatory compliance understanding
- Team collaboration skills
Candidates with exposure to pharmaceutical, nutraceutical, cosmetic, or healthcare clinical studies will have an added advantage.
Salary Estimate
Based on current CRO and Clinical Research industry standards in Ahmedabad, the estimated salary range for this Project Coordinator role is:
Estimated Salary Range
₹4.5 LPA – ₹7.5 LPA
Salary may vary depending on:
- CRO experience
- Clinical research exposure
- Documentation expertise
- Regulatory knowledge
- Interview performance
Additional career benefits may include exposure to regulated clinical studies, operational growth opportunities, and experience in healthcare compliance systems.
Why Apply for This CRO Project Coordinator Job?
This NovoBliss Research opportunity provides strong career growth for professionals interested in clinical operations and project coordination.
Career Benefits
- Exposure to real clinical research projects
- Experience in CRO operations
- Growth in clinical project management
- Regulatory compliance exposure
- Opportunity to work with GCP and CDSCO guidelines
- Experience in study coordination and documentation systems
- Learning opportunities in healthcare quality systems
Professionals with clinical operations experience can significantly strengthen their careers through this role.
Interview Details
Company Name
NovoBliss Research Private Limited
Position
Project Coordinator
Industry
Clinical Research / CRO
Job Type
Full-Time
Work Location
Ahmedabad, Gujarat
Work Mode
On-site
Apply Mode
Online Application
How to Apply
Interested candidates can apply online through the official LinkedIn application link.
Candidates are advised to apply early and keep their updated resumes ready before submission.
Required Documents
Candidates should keep the following documents prepared before applying:
- Updated Resume/CV
- Educational Certificates
- Government ID Proof
- Experience Certificates
- Passport-size Photograph
- Current Salary Details (if applicable)
- Clinical Research Certifications (if available)
- Updated LinkedIn Profile
- Contact Information
It is recommended to prepare an ATS-friendly resume focused on Clinical Research and CRO Operations skills.
Frequently Asked Questions (FAQs)
1. What is the job role offered by NovoBliss Research?
NovoBliss Research is hiring for the role of Project Coordinator in Clinical Research and CRO Operations.
2. What qualifications are required for this role?
Candidates with B.Pharm, M.Pharm, Life Sciences, or related qualifications can apply.
3. Is CRO experience mandatory?
Candidates with prior CRO or Clinical Research experience will be preferred.
4. What is the location of the job?
The job location is Ahmedabad, Gujarat, India.
5. What guidelines and regulations should candidates know?
Knowledge of GCP, CDSCO regulations, and ISO 9001:2015 standards is preferred.
6. What is the estimated salary range?
The estimated salary range is ₹4.5 LPA – ₹7.5 LPA.
7. Is this a remote job?
No, this is an on-site full-time position.
8. What industries does NovoBliss Research work with?
The company works with pharmaceutical, nutraceutical, cosmetic, OTC, dental, and healthcare sectors.
Final Conclusion
NovoBliss Research has opened an excellent career opportunity for professionals interested in Clinical Research, CRO Operations, and Project Coordination. This Ahmedabad-based Project Coordinator role offers strong exposure to study management, regulatory compliance, documentation systems, and clinical trial operations.
Candidates with experience in clinical research workflows, CRO coordination, GCP compliance, and healthcare documentation systems can significantly benefit from this opportunity.
Working in a CDSCO-registered and ISO-certified CRO environment can help professionals strengthen their long-term careers in Clinical Operations, Regulatory Affairs, and Healthcare Project Management.
Candidates interested in advancing their clinical research careers should consider applying for this opportunity as early as possible.
Disclaimer
This job information is provided for educational and informational purposes only. Candidates are advised to verify all recruitment details from the official company website or official job portal before applying. Pharma Duniya is not responsible for recruitment processes, interview schedules, or hiring decisions made by the company
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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