Cliantha Research Hiring For Medical Writer

Cliantha Research, a leading Clinical Research Organization (CRO), is inviting applications for the position of Medical Writer at its Ahmedabad office. This is an excellent opportunity for B.Pharm and M.Pharm professionals with 2–4 years of experience who are looking to build a rewarding career in Clinical Research, Medical Writing, Protocol Development, and Regulatory Documentation.

If you have expertise in medical writing, protocol preparation, GCP, GLP, and regulatory documentation, this opportunity offers excellent career growth in a professional CRO environment.

Cliantha Research is a globally recognized Clinical Research Organization (CRO) providing comprehensive clinical research services across pharmaceuticals, biotechnology, medical devices, and healthcare sectors. The company is known for maintaining high standards of regulatory compliance, quality, and scientific excellence.

Selected candidates will be responsible for:

• Preparing clinical study protocols and protocol-related documentation.
• Drafting Informed Consent Documents (ICDs) and Case Report Forms (CRFs).
• Coordinating with Principal Investigators, Sponsors, Biostatisticians, Analytical Investigators, and study teams.
• Managing protocol revisions and documentation updates.
• Coordinating Ethics Committee submissions and approvals.
• Translating Gujarati Informed Consent Documents from English to Gujarati.
• Communicating protocol amendments with investigators and sponsors.
• Preparing and updating Standard Operating Procedures (SOPs).
• Ensuring compliance with GCP, GLP, FDA, and applicable regulatory guidelines.
• Maintaining protocol documentation according to company SOPs.

Educational Qualification

Candidates should possess:

Experience Required

• 2–4 years of Medical Writing or Clinical Research experience.

Candidates with the following skills will be preferred:

• 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
• Excellent scientific writing skills
• Strong communication and coordination abilities

Working with Cliantha Research offers:

• Opportunity to work with an established Clinical Research Organization.
• Exposure to global clinical research projects.
• Career growth in Medical Writing and Regulatory Documentation.
• Hands-on experience with protocol preparation and ethics submissions.
• Professional learning environment.
• Competitive salary and employee benefits.

Ahmedabad, Gujarat

This is an On-Site position.

Based on experience and industry standards, the expected salary is:

₹4.0 – ₹5.5 LPA

(Final compensation will depend on qualifications and interview performance.)

Application Link