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4 days ago
**MakroCare** is an 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**Job description**:
- ** Medical**
**Writer (CER)**
- Writing and reviewing clinical/regulatory documents such as clinical trial protocols, Clinical evaluation reports, investigator brochures, informed consent forms, and according to ICH or other guidelines.
- CER (Clinical Evaluation) Module Drafting & Documentation writing.
- 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.
**Education & Qualifications**:
- Any Bachelor / Masters in Life Sciences Only
- Required: a Minimum of **2-6** years of experience in **Medical Writing** (CER) or a related field.
- We looking for those who join immediately
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Medical Writing Coordinator
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