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Job Location | Hyderabad |
Education | Not Mentioned |
Salary | Not Disclosed |
Industry | Medical / Healthcare |
Functional Area | Allied Health Services |
EmploymentType | Full-time |
Greetings From Indegene Private Limited !Job Description -Responsible for authoring clinical evaluation reports, clinical evaluation plans, post-market surveillance reports, and periodic safety update reportsLiterature search, screening, and summarization of articlesPerform data fact check of the documents authoredEnsure documents comply with the client/regulatory requirementsParticipate in client calls per project requirementsCompliance to quality, confidentiality, and securityAdhere and follow quality systems, processes and policiesComply to training and specificationsMinimum of 1 year experience in any of the following functions scientific writing/regulatory-medical writing/developing/publishing medical contentUnderstanding of medical devices (preferred) or an overall understanding of the medical field.Strong flair and passion for writing.Strong written and verbal communication/presentation skills.Passion for networking.Being up-to-date with the latest technical/scientific developments and relating them to various projects.Any Life science or biomedical graduate with 1 to 2 years of experience
Keyskills :
medical devicesscientific writingmedical writingpublishingclinical evaluation planclinical evaluation report