Medical Writer
Cliantha Research is hiring Medical Writers for its Ahmedabad office. This full-time opportunity is ideal for B.Pharm and M.Pharm professionals with experience in Medical Writing, Clinical Research, Protocol Development, Regulatory Documentation, and Clinical Trial Documentation.
Candidates with strong scientific writing skills and experience in protocol preparation, GCP, GLP, CRFs, ICDs, and SOP development are encouraged to apply.
📋 Job Overview
| Particular | Details |
|---|---|
| Company | Cliantha Research |
| Position | Medical Writer |
| Department | Research & Development |
| Industry | Clinical Research / CRO |
| Location | Ahmedabad, Gujarat |
| Employment Type | Full-Time, Permanent |
| Qualification | B.Pharm / M.Pharm |
| Experience | 2–4 Years |
| Vacancy | 1 |
💼 Key Responsibilities
- Prepare clinical study protocols and protocol-related documents.
- Draft Informed Consent Documents (ICDs).
- Prepare Case Report Forms (CRFs).
- Coordinate with Principal Investigators, Sponsors, and study teams.
- Manage protocol revisions and documentation updates.
- Coordinate Ethics Committee submissions and approvals.
- Translate Gujarati ICDs from English to Gujarati.
- Communicate protocol amendments with investigators and sponsors.
- Prepare and update Standard Operating Procedures (SOPs).
- Ensure compliance with GCP, GLP, FDA, and regulatory guidelines.
- Maintain protocol documentation as per company SOPs.
🎓 Eligibility Criteria
- B.Pharm
- M.Pharm
- 2–4 Years of Medical Writing or Clinical Research experience.
🧠 Preferred Skills
- Medical Writing
- Protocol Writing
- Clinical Protocol Development
- Case Report Forms (CRFs)
- Informed Consent Documents (ICDs)
- Clinical Study Reports
- Good Clinical Practice (GCP)
- Good Laboratory Practice (GLP)
- Regulatory Documentation
- SOP Preparation
- Clinical Trial Documentation
- Scientific Writing
- Communication & Coordination Skills
This opportunity allows Medical Writing professionals to work on clinical protocols, regulatory documentation, ethics submissions, and global clinical research projects within a leading Clinical Research Organization.
💰 Salary & Benefits
Based on industry standards and the information provided for this position:
Estimated Salary: ₹4.0 – ₹5.5 LPA
Final compensation will depend on qualifications, experience, and interview performance.
Employee Benefits
- Opportunity to work with an established Clinical Research Organization (CRO).
- Exposure to Global Clinical Research Projects.
- Career Growth in Medical Writing & Regulatory Documentation.
- Hands-on Experience in Protocol Development.
- Professional Learning Environment.
- Competitive Compensation & Employee Benefits.
🌟 Why Join Cliantha Research?
- Work with an internationally recognized CRO.
- Gain experience in Protocol Writing and Clinical Documentation.
- Exposure to Ethics Committee submission processes.
- Build expertise in Regulatory Documentation.
- Work closely with Sponsors, Investigators, and Clinical Teams.
- Excellent career growth in Clinical Research and Medical Writing.
📈 Career Growth Opportunities
- Senior Medical Writer
- Clinical Research Associate (CRA)
- Regulatory Affairs Associate
- Clinical Documentation Specialist
- Medical Writing Lead
- Clinical Project Coordinator
- Regulatory Documentation Manager
- Medical Affairs Professional
📑 Resume Tips
- Highlight Medical Writing and Clinical Research experience.
- Mention Protocol Writing and CRF preparation.
- Include GCP, GLP, and Regulatory Documentation knowledge.
- Showcase SOP preparation experience.
- Mention scientific writing and communication skills.
- Keep your resume ATS-friendly.
🎯 Interview Questions
- What is Medical Writing?
- What are Clinical Study Protocols?
- Explain the purpose of an Informed Consent Document (ICD).
- What is a Case Report Form (CRF)?
- What is Good Clinical Practice (GCP)?
- What is Good Laboratory Practice (GLP)?
- How do you manage protocol amendments?
- Why do you want to join Cliantha Research?
- How do you ensure accuracy in scientific documents?
- Tell us about your Medical Writing experience.
📌 How to Apply?
Interested and eligible candidates can apply online through the official application link.
🚀 Apply Now
Apply Online📚 Related Resources from Medical Jobs India
❓ Frequently Asked Questions
Q. Who can apply for this position?
Candidates with B.Pharm or M.Pharm qualifications and 2–4 years of Medical Writing or Clinical Research experience can apply.
Q. Where is the job location?
Ahmedabad, Gujarat.
Q. Is this a permanent position?
Yes. It is a full-time permanent role.
Q. What is the expected salary?
₹4.0–₹5.5 LPA (Estimated).
Q. What are the major responsibilities?
Protocol writing, ICD and CRF preparation, SOP development, Ethics Committee coordination, and Regulatory Documentation.
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