Medical Writer/ Clinical Study Researcher

Open for Delhi and Bangalore location only

• Proficient in developing high-quality key clinical trial documents, including protocols, Investigator's Brochures (IBs)
• Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).
• Proficient in translating complex scientific data into clear, regulatory compliant documents that support drug development and approval processes.
• Additionally, experienced in crafting abstracts and manuscripts, demonstrating strong scientific communication skills.
• Committed to delivering high-quality, accurate, and well-structured documents that contribute to the success of clinical research and regulatory submissions.
• Preparation of protocols, CSRs, PIS-ICFs and CRFs.
• Understanding the study objectives and designing the protocol.
• Preparation and review of SOPs.
• Communicating with all stakeholders to ensure effective and complete documentation within the timeline.