Explore medical writer jobs in clinical research and pharma at Cliantha Research. Join as Medical Writer with 2-4 years experience in protocol writing. Grow your career in regulatory medical writing today!
Contents
About the Company
Cliantha Research is a full-service Contract Research Organization (CRO) headquartered in Ahmedabad, India, with global operations across North America, Europe, and Asia.
Specializing in clinical trials, bioanalytical services, dermatology, first-in-human studies, and regulatory support, Cliantha delivers end-to-end solutions for pharmaceutical, biotechnology, and consumer health companies.
With state-of-the-art facilities and a strong focus on quality, compliance, and innovation, Cliantha adheres to global regulatory standards including USFDA, Health Canada, and ICH-GCP.
Backed by a dedicated team of experts, the company accelerates drug development while ensuring patient safety and data integrity worldwide.
Job Details
- Company Name: Cliantha Research
- Experience: 2-4 Years
- Qualification: B.Pharm
- Location: Cliantha Corporate (Ahmedabad, Gujarat)
- Work Type: On-site
Job Description
Cliantha Research is hiring experienced professionals for its Medical Writing Department.
This role involves preparing essential clinical trial documents in compliance with regulatory guidelines. Collaborate with cross-functional experts to support high-quality study documentation.
Medical Writer
- Department: Medical Writing
- Role: Medical Writer (Protocol & Regulatory Documents)
- Experience: 2-4 Years
- Education/Qualification: B.Pharm
Skills/Qualifications
- B.Pharm degree with strong academic background
- 2-4 years experience in medical writing
- Expertise in regulatory document preparation
- Knowledge of ICH-GCP and applicable guidelines
- Excellent scientific writing and communication skills
- Attention to detail and regulatory compliance awareness
- Ability to collaborate with multidisciplinary teams
Key Responsibilities
- Prepare clinical study protocols
- Develop Informed Consent Documents (ICDs)
- Design Case Report Forms (CRFs)
- Create other protocol-related documents
- Ensure compliance with regulatory requirements
- Consult with Principal Investigators and Biostatisticians
- Coordinate with Analytical Investigators and department heads
- Maintain document accuracy and quality standards
Benefits/Perks
- Competitive salary with performance incentives
- Comprehensive health and wellness benefits
- Professional development and training programs
- Exposure to global clinical research projects
- Collaborative and ethical work environment
- Career progression in medical writing and regulatory affairs
- Stability with a leading CRO
How to Apply
Interested candidates can apply through the official Cliantha Research careers portal or job portals listing this position (Job Code/Reference: Med–2025-11-21-971).
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Cliantha Research Career page.
Update your CV highlighting medical writing experience and email to the recruitment team if specified on the portal. For more clinical research and medical writing opportunities, visit Pharma Recruiter. Advance your regulatory writing career—apply now!
Why You Should Join
Cliantha Research offers a dynamic environment for medical writers passionate about clinical research. As a globally recognized CRO, it provides exposure to diverse therapeutic areas and cutting-edge studies.
Employees benefit from collaborative teamwork, continuous learning, and opportunities to contribute to innovative drug development. With strong regulatory compliance and patient-centric focus, Cliantha ensures long-term career growth and professional recognition.
FAQs
What qualifications are required for the Medical Writer role at Cliantha?
B.Pharm with 2-4 years of experience in medical writing, preferably in clinical protocols and regulatory documents.
Is this medical writer position open to freshers?
No, it requires a minimum of 2 years and maximum 4 years of relevant experience.
Where is the Medical Writer job located?
Cliantha Corporate Office in Ahmedabad, Gujarat (on-site role).
What documents will I work on as a Medical Writer?
Primarily protocols, informed consent forms, CRFs, and other regulatory-compliant study documents.