A leading organization in the clinical research and medical devices sector is hiring an experienced Medical Writer / Clinical Researcher for Ahmedabad and remote roles. This opportunity is ideal for professionals with 3–5 years of experience in medical writing, clinical trials documentation, and regulatory writing.

If you have expertise in clinical study reports (CSR), protocol writing, ICF development, and regulatory compliance, this role offers strong career growth in the pharmaceutical and healthcare industry.

Job Overview

• Role: Medical Writer / Clinical Researcher
• Location: Ahmedabad / Remote
• Experience: 3–5 Years
• Industry: Clinical Research | Pharmaceuticals | Healthcare
• Employment Type: Full-Time

Key Responsibilities

• Develop and write clinical study reports (CSR), protocols, SOPs, and plain language summaries
• Create scientific content, blogs, articles, and publications
• Prepare manuscripts, abstracts, literature reviews, and white papers
• Collaborate with clinical research, regulatory affairs, safety, and biostatistics teams
• Ensure compliance with ICH-GCP, FDA, EMA, PMDA, and ICMR guidelines
• Conduct systematic literature reviews and data analysis
• Edit and proofread medical documents for accuracy and clarity
• Support training materials and scientific communication projects
• Stay updated on clinical trials, drug development, and regulatory trends

Qualifications & Skills

• Bachelor’s or Master’s degree in:
  • Life Sciences
  • Pharmacy (B.Pharm / M.Pharm)
  • Biotechnology
  • Medicine or related field
• 3–5 years of experience in:
  • Medical writing
  • Clinical research documentation
  • Regulatory writing (IND, NDA, CTD modules)
• Strong understanding of:
  • Clinical trial processes
  • Medical terminology
  • Regulatory requirements
• Proficiency in:
  • MS Office (Word, Excel, PowerPoint)
  • Reference management tools
• Excellent:
  • Scientific writing skills
  • Data interpretation and analysis

Preferred Qualifications

• Familiarity with ICMJE and GPP3 publication guidelines
• Hands-on experience in:
  • Clinical study reports (CSR)
  • Investigational New Drug (IND) applications
  • New Drug Applications (NDA)

Why Apply for This Medical Writer Job?

• Work with leading experts in clinical research and medical devices
• Gain exposure to global regulatory writing and clinical trials
• Opportunity to build a career in pharmaceutical medical writing
• Dynamic and growth-oriented work environment
• Remote flexibility with strong career advancement potential

How to Apply

Interested candidates can share their updated resume at:
📧 rahulkumar.cr@merillife.com