CER Medical Writing Full Time

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

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