A medical/scientific/academic writer.
Clinical and Non-Clinical
• Drafting/quality check of Module 2 Common Technical Documents like Non-Clinical Overview (Module 2.4), Non-clinical summary (Module 2.6) and supporting IND projects.
• Writing newsletters, writing clinical study protocol, informed consent form, investigators brochure.
• Write and edit clinical study documents
• Perform independent peer review/ QC of several medical writing documents
• Key areas:
? Gene therapy, immuno-oncology, stem cell therapy, radiopharmaceutical and radio-diagnostic.
? To perform literature reviews including the retrieval and analysis of data, study design terms, competitive product pipeline information, epidemiology trends, treatment patterns etc.
? Process clinical trial data (Phase I to IV including observational studies) and abstracting clinical information providing supporting and related information for required analysis.