🚀 Build Your Career in Medical Device Clinical Research
Are you passionate about clinical research, medical devices, or regulatory affairs? Here’s an exciting opportunity to work with one of India’s leading medical technology companies. Meril Medical Innovation Sciences Pvt. Ltd. is inviting applications for the position of Clinical Trial Assistant (CTA) / Clinical Trial Associate at its Vapi, Gujarat facility.
If you have experience in clinical research, medical writing, regulatory documentation, or medical devices, this role offers an excellent chance to work on global clinical evaluation projects while contributing to innovative healthcare solutions.
🏢 About Meril Medical Innovation Sciences Pvt. Ltd.
Meril Medical Innovation Sciences Pvt. Ltd. is a globally recognized Indian medical device company headquartered in Vapi, Gujarat. Since its establishment, the company has developed advanced medical technologies across multiple specialties, including cardiovascular devices, orthopedics, endo-surgery, robotics, diagnostics, and healthcare innovations.
With products available in more than 100 countries, Meril focuses on research, innovation, quality manufacturing, and regulatory excellence. Working at Meril gives professionals exposure to international standards, cutting-edge technologies, and a collaborative research environment.
📌 Job Overview
| Particular | Details |
|---|---|
| Company | Meril Medical Innovation Sciences Pvt. Ltd. |
| Job Role | Clinical Trial Assistant (CTA) / Clinical Trial Associate |
| Location | Vapi, Gujarat |
| Experience Required | 1–5 Years |
| Employment Type | Full-Time |
| Industry | Medical Devices / Clinical Research |
| Department | Clinical Evaluation & Regulatory Affairs |
🎯 Key Responsibilities
As a Clinical Trial Assistant or Associate, you will support clinical evaluation activities and regulatory documentation for medical devices.
📄 Clinical Evaluation Report (CER) Preparation
- Assist in preparing and updating Clinical Evaluation Reports (CERs).
- Compile scientific evidence supporting medical device safety and performance.
- Ensure documentation complies with regulatory guidelines.
🔬 Literature Review & Clinical Research
- Conduct literature searches using scientific databases.
- Review published clinical studies and safety information.
- Summarize research findings for regulatory documentation.
📑 Regulatory Documentation
- Support preparation of documents for CDSCO submissions.
- Maintain technical files and regulatory records.
- Coordinate documentation required for approvals.
🧪 Biological Evaluation
- Assist in preparing Biological Evaluation Plans and Reports.
- Support activities related to ISO 10993 biocompatibility evaluations.
- Coordinate testing documentation with laboratories.
🤝 Laboratory & Post-Market Surveillance Support
- Communicate with external testing laboratories.
- Track testing timelines and reports.
- Assist in Post-Market Surveillance (PMS) documentation and safety reporting.
🎓 Eligibility Criteria
Candidates should possess:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, Biomedical Sciences, or a related discipline.
- 1–5 years of relevant experience.
- Experience in clinical research, medical writing, regulatory affairs, or medical devices.
- Strong analytical and documentation skills.
- Good communication and coordination abilities.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
Preferred Skills
Candidates with experience in the following areas will have an advantage:
- Clinical Evaluation Reports (CER)
- Medical Device Documentation
- CDSCO Regulatory Submissions
- Scientific Literature Review
- ISO 10993 Biological Evaluation
- Post-Market Surveillance (PMS)
🌟 Why Join Meril?
Working with Meril offers numerous professional growth opportunities:
- 🌍 Exposure to global medical device regulations.
- 📚 Learn advanced Clinical Evaluation and Regulatory Affairs.
- 🔬 Work on innovative healthcare technologies.
- 🚀 Career growth in one of the fastest-growing medical device companies.
- 🤝 Collaborate with experienced researchers and regulatory professionals.
- 📈 Gain valuable experience in international medical device compliance.
💼 Who Should Apply?
This opportunity is ideal for professionals working in:
- Clinical Research
- Medical Writing
- Regulatory Affairs
- Medical Devices
- Pharmacovigilance
- Biomedical Research
- Scientific Documentation
Candidates looking to transition into the medical device industry will also find this role highly rewarding.
📧 How to Apply
Interested candidates can send their updated resume to the HR team.
Email IDs:
Suggested Email Subject
Application for Clinical Trial Assistant / Associate – Your Name – X Years Experience
Before applying, ensure your resume highlights:
- Clinical research experience
- Medical writing projects
- Regulatory documentation
- Literature review experience
- CER or CDSCO exposure (if applicable)
💡 Career Tip
Medical device regulatory affairs is one of the fastest-growing career domains in healthcare. Professionals with expertise in Clinical Evaluation Reports (CER), ISO 10993, and regulatory documentation are increasingly in demand across India, Europe, and the United States. Developing these skills can significantly enhance your long-term career prospects.
🔍 Frequently Asked Questions (FAQs)
1. Is this position open for freshers?
No. The company is seeking candidates with 1 to 5 years of relevant experience in clinical research, regulatory affairs, medical writing, or medical devices.
2. Where is the job located?
The position is based in Vapi, Gujarat, and is an on-site role.
3. What qualifications are preferred?
Candidates from Pharmacy, Life Sciences, Biotechnology, Biomedical Engineering, or related fields with relevant experience are encouraged to apply.
4. What are the important skills for this role?
Knowledge of Clinical Evaluation Reports (CER), literature review, CDSCO submissions, ISO 10993, medical writing, and regulatory documentation will be highly beneficial.
5. How can I apply?
Send your updated CV to:
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