Overview:

- MakroCare is expert strategic development and commercialization global partner for the 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 Jr Level

- If the candidate is fresher need to train in Medical Writer field ( or any related field)

- Writing and reviewing clinical/regulatory documents such as clinical trial protocols, clinical study reports, investigator brochures, informed consent forms, and according to ICH or other guidelines.

- Minimum of 1-3 years of experience.

- Module Drafting (2.4, 2.5. 2.6 & 2.7).

- Publication manuscripts, abstracts, posters (content writing) and presentations

- To 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.

Website: http://www.makrocare.com

Industry: Pharmaceutical Manufacturing

Company size : 501-1,000 employees

MakroCare has operations and presence in US, UK, EU, and Asia. MakroCare is well-positioned to meet the demands of the expanding product portfolio needs of our life sciences clients worldwide. We also understand the demands of an increasingly competitive market.

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