Responsible for authoring clinical evaluation reports, clinical evaluation plans, post-market surveillance reports, and periodic safety update reports
Literature search, screening, and summarization of articles
Perform data fact check of the documents authored
Ensure documents comply with the client/regulatory requirements
Participate in client calls per project requirements
Compliance to quality, confidentiality, and security
Adhere and follow quality systems, processes and policies
Comply to training and specifications
Minimum of 1 year experience in any of the following functions scientific writing/regulatory-medical writing/developing/publishing medical content
Understanding 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
This job is provided by Shine.com
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