Medical Writer – Clinical Research
Scientific & Regulatory Affairs · Bengaluru (on-site) · Reports to the Manager, Scientific & Regulatory Affairs

About the role
You will write and review the documents that run a clinical study. That means protocols, consent forms, study reports and papers. You will make sure each one is correct, clear and follows the rules.
If you have helped investigators turn a study idea into a protocol, or turned trial results into a paper, this job is for you.

What you will do
• Write and review study protocols, clinical study reports (CSRs), statistical analysis plans (SAPs), investigator brochures and informed consent documents.
• Write and review manuscripts, abstracts, posters and presentations.
• Prepare documents for ethics committees and regulators.
• Check that every document is scientifically correct and consistent with the protocol.
• Make sure documents follow ICH-GCP, CDSCO requirements,



the New Drugs and Clinical Trials Rules 2019 and the Medical Devices Rules 2017.
• Handle several documents and deadlines at the same time.
• Able to travel for work about 10% of the time.

What you bring
• A Masters degree in Medicine or Dentistry
• 4–5 years of medical or scientific writing, including regulatory documents.
• A positive grasp of clinical research, GCP, study design and basic statistics.
• Clear, careful writing. Good planning. Calm under deadlines.

Good to have
• Experience working with academic investigators or research institutions.
• Papers published in peer-reviewed journals.

How to apply
Apply on LinkedIn. Please attach one writing sample (a protocol section, report extract or published paper you wrote). Remove any confidential details.

📌 Medical Writer – Clinical Research (Bengaluru)
🏢 TrialGuna Private
📍 Bengaluru