Job description: Medical Writer Jr Level

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

• Minimum of 0.6 - 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 devicegroups or subgroups.

• Develop templates for reports and other regulatory documents.

Educational Qualification: BDS or MDS or D Pharma or M-Pharma or MSc or any science background

Skills required: Microsoft Word Alignments, CSR (clinical study report) Drafting & Module Drafting (2.4, 2.5. 2.6 & 2.7)

MakroCare  (https://www.makrocare.com/) is 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.

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.