Are you a skilled Medical Writer with expertise in protocol writing and regulatory documentation? Biosite Research, a leading clinical research organization (CRO) based in Bangalore, is looking for a talented professional to join our team.
If you have 3–4 years of experience in medical writing, particularly in clinical research protocols, ICH-GCP guidelines, and regulatory submissions, this could be the perfect opportunity for you!
📝 Job Description
As a Medical Writer at Biosite Research, you will:
✔ Develop and review clinical trial protocols, study reports, and regulatory documents
✔ Ensure compliance with ICH-GCP, FDA, EMA, and other regulatory guidelines
✔ Collaborate with researchers, biostatisticians, and regulatory teams
✔ Prepare investigator brochures, informed consent forms (ICFs), and clinical study reports (CSRs)
✔ Edit and proofread scientific documents for accuracy, clarity, and consistency
🏢 About Biosite Research
Biosite Research is a growing CRO specializing in clinical research, regulatory submissions, and medical writing. We work with pharmaceutical companies, biotech firms, and research institutions to deliver high-quality documentation that meets global standards.
🔹 Why Join Us?
✅ Work on cutting-edge clinical research projects
✅ Be part of a collaborative and innovative team
✅ Opportunities for career growth and skill development
📩 How to Apply
If you are passionate about medical writing and meet the requirements, we’d love to hear from you!
📌 Send your updated CV to: hr@biositeindia.com
