1+ year Contract
> Review and update protocols, case report forms, informed consent forms, and clinical study reports.
> Review and update or update Clinical Evidence Summaries/Clinical Evaluation Reports, Risk-benefit analysis reports, Post-market Surveillance documentation
> Attend medical and project team meetings and client teleconferences as required
> Demonstrates sound knowledge of the medical writing process, medical device regulations, and associated approval processes
> Applies medical concepts and terminology appropriately
> Updates project-related tracking tools
> Ability to work with multiple teams to collect documents as required
> Maintains records for all assigned projects, including archiving
> Schedules and conducts document-related meetings, including the preparation of meeting agendas, key data points for discussion, and meeting minutes
If interested please do let me know.
I'll get back to you with you more details.
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Fusion Life Sciences Technologies LLC
Direct - 678 882 1439