Meril Life Sciences is inviting applications for the position of Medical Writer – Clinical Research in Ahmedabad, Gujarat. This on-site opportunity is suitable for fresh graduates and candidates with up to one year of relevant experience in medical writing or clinical research.
The role focuses on preparing clinical study documents, reviewing scientific literature, and supporting clinical research related to IVF Media and Assisted Reproductive Technology (ART). Candidates with a background in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related discipline can consider applying.
This opportunity may be suitable for candidates looking to begin a career in clinical research documentation, scientific writing, and regulatory-compliant clinical study processes.
Meril Life Sciences Recruitment 2026: Job Highlights
| Particulars | Details |
|---|---|
| Company | Meril Life Sciences |
| Job Title | Medical Writer – Clinical Research |
| Job Location | Ahmedabad, Gujarat |
| Work Mode | On-site |
| Experience | Freshers / Up to 1 year |
| Qualification | Bachelor’s or Master’s degree in a relevant field |
| Eligible Fields | Life Sciences, Pharmacy, Biotechnology, Clinical Research, or related disciplines |
| Research Area | IVF Media and Assisted Reproductive Technology (ART) |
| Salary | Not specified in the available vacancy details |
| Application Mode | |
| Application Email | rahulkumar.cr@merillife.com |
About Meril Life Sciences
Meril Life Sciences operates in the healthcare and medical technology sector. The advertised position focuses on clinical research documentation and scientific writing in the area of IVF Media and Assisted Reproductive Technology.
The role offers an opportunity for eligible candidates to develop skills in clinical study documentation, scientific literature evaluation, and coordination with clinical research teams.
Job Description: Medical Writer – Clinical Research
The Medical Writer will support clinical research activities by preparing, reviewing, and maintaining clinical study documents. The position requires attention to scientific accuracy, consistency, document quality, and compliance with relevant clinical research requirements.
The selected candidate will also review published scientific evidence and coordinate with Clinical Operations, Regulatory Affairs, Biostatistics, and Data Management teams to support the timely completion of clinical study documentation.
Key Responsibilities
1. Clinical Study Documentation
- Prepare and maintain clinical research documents, including study protocols, Informed Consent Forms (ICFs), and Case Report Forms (CRFs).
- Support the preparation and organization of other essential clinical study documents.
- Review documents for completeness, clarity, accuracy, and consistency.
- Incorporate feedback from reviewers and support document finalization.
2. Scientific Literature Review
- Conduct literature searches relevant to IVF Media and Assisted Reproductive Technology.
- Evaluate scientific publications and available evidence.
- Organize research findings to support clinical study documentation.
- Ensure that scientific information is presented accurately and clearly.
3. Regulatory Compliance and Quality
- Follow applicable ICH-GCP principles and relevant regulatory requirements.
- Maintain document consistency and version control.
- Support the review and correction of documentation comments.
- Help ensure that clinical research records meet established quality expectations.
4. Cross-Functional Collaboration
- Coordinate with Clinical Operations, Regulatory Affairs, Biostatistics, and Data Management teams.
- Communicate document updates and review comments to relevant stakeholders.
- Support the timely completion of clinical study documentation.
- Assist with maintaining organized and accurate study records.
Eligibility Criteria
Educational Qualification
Candidates should have a bachelor’s or master’s degree in one of the following fields or a related discipline:
- Life Sciences.
- Pharmacy.
- Biotechnology.
- Clinical Research.
- Other relevant scientific or healthcare-related fields.
Experience Required
- Freshers can apply.
- Candidates with up to one year of relevant experience in clinical research or medical writing are also eligible according to the vacancy listing.
A basic understanding of clinical study documentation and ICH-GCP is expected.
Additional Advantage
Exposure to any of the following areas may be beneficial:
- IVF and Assisted Reproductive Technology.
- Reproductive medicine.
- Medical device clinical studies.
- Clinical research documentation.
- Scientific literature review.
Required Skills
Applicants should ideally demonstrate the following skills:
- Scientific writing and documentation.
- Literature search and evidence evaluation.
- Strong written and verbal communication.
- Analytical thinking and attention to detail.
- Understanding of clinical research documentation.
- Familiarity with ICH-GCP principles.
- Document review and version control.
- Organizational skills and deadline management.
- Ability to work with cross-functional teams.
Job Location and Work Mode
The position is based in Ahmedabad, Gujarat, India, and is listed as an on-site role.
Candidates should consider the location before applying and confirm the exact office address, working hours, and other employment conditions with the recruitment contact.
Salary and Benefits
The salary package and employee benefits have not been specified in the available vacancy announcement. Candidates can contact the recruitment representative to confirm compensation, working hours, and other employment terms.
How to Apply for Meril Life Sciences Recruitment 2026
Interested candidates can send their updated CV to the email address listed in the vacancy announcement.
Application Email: rahulkumar.cr@merillife.com
Application Tips
- Prepare an updated resume highlighting your educational qualifications and relevant academic projects.
- Mention Medical Writer – Clinical Research Application in the email subject.
- Highlight any training or experience in scientific writing, literature review, clinical research, or ICH-GCP.
- Include relevant exposure to IVF, ART, or medical device clinical studies, if applicable.
- Attach your CV in PDF format and ensure your contact details are correct.
Frequently Asked Questions (FAQs)
1. Which company is hiring Medical Writers?
Meril Life Sciences is listed as the recruiting company for the Medical Writer – Clinical Research position.
2. Where is the job located?
The position is based in Ahmedabad, Gujarat.
3. Can freshers apply?
Yes. The vacancy listing states that freshers can apply.
4. What is the required qualification?
A bachelor’s or master’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related field is required.
5. How much experience is needed?
Freshers and candidates with up to one year of relevant experience may apply.
6. What is the main research area for this role?
The role supports clinical research related to IVF Media and Assisted Reproductive Technology (ART).
7. What documents will the Medical Writer work on?
The listed documents include clinical study protocols, Informed Consent Forms, Case Report Forms, and other essential study documents.
8. Is ICH-GCP knowledge important?
Yes. A basic understanding of ICH-GCP and clinical study documentation is included in the eligibility details.
9. What is the salary for this job?
The salary has not been disclosed in the available vacancy information.
10. How can candidates apply?
Candidates can email their updated CV to rahulkumar.cr@merillife.com.
Disclaimer
This article is a rewritten summary of a third-party vacancy listing. Vacancy status, eligibility criteria, salary, and application instructions may change. Candidates should verify the latest details with Meril Life Sciences or the listed recruitment contact before applying.