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Job Opportunity at
Clinical Dynamix, Inc.
Posted on Oct 29
Essential Job Functions
Serve as the lead Clinical / Medical Report Writer contributing to a variety of documents for clinical research and regulatory purposes, including clinical research protocols, annual and final study reports, investigator’s brochures, and regulatory submissions including clinical summary reports (CSR), clinical evaluation (CER), and post-market surveillance (PMS) reports.
Coordinate the efforts of cross-functional teams to produce high-quality, scientifically accurate documents.
Manage timelines and communicate with team members to maintain awareness of expectations, milestones, and deliverables.
Review and assist in preparation of scientific publications.
Prepare basic statistical analysis reports as needed.
Minimum of bachelor’s Degree or equivalent in scientific or medical discipline; Master's Degree preferred
Minimum of four years medical writing experience
Experience with medical devices a plusmedical
Excellent written communication skills
Experience producing high quality medical, clinical and technical documents
Basic project management and organizational skills
Ability to prioritize and manage multiple projects
Impeccable attention to detail related to consistency, grammar, syntax, and accuracy
Strong familiarity with Microsoft Office
Experience and skill performing medical literature searches (PubMed, Google Scholar, etc.) highly preferred
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