MakroCare Expert Strategic Development and Commercialization Global Partner for Pharmaceutical, Biotechnology and Medical Device industries. Our Experience, Programs and Processes bring a New Dimension to Development Strategy, Regulatory/Risk Planning & Management, Clinical Research, Medical/Scientific Support and Emerging Region Expansion.
Post : Medical Writer (CSR)
• Writing and reviewing clinical/regulatory documents such as clinical trial protocols, clinical study reports (CSR), investigator brochures, informed consent forms, and according to ICH or other guidelines.
• Module Drafting (2.4, 2.5. 2.6 & 2.7).
• Publication manuscripts, abstracts, posters (content writing) and presentations participate in post-market surveillance activities by conducting routine systematic literature reviews (e.g. Screening of articles against inclusion/exclusion criteria, extracting data from included studies,
• interpreting study results and preparing summaries into formal reports) for specific medical device groups or subgroups.
• Develop templates for reports and other regulatory documents.
• Any UG/PG in Life Science background
• Minimum of 1-3 years of experience in the Medical Writing with in CSR field.
Experience : 1-3 years
Qualification : UG/PG in Life Science background
Location : Hyderabad - Madhapur
Industry Type : Pharma/ Healthcare/ Clinical research
Last Date : 24th Sepetmber, 2023
See All Other Jobs in our Database