Job Description:
• Author and maintain clinical and post-market documentation
• Ensure adherence to Good Documentation Practices
• Handle development of clinical evaluation deliverables
• Compile and synthesize data types for evaluations
• Collaborate to generate compliant documents
• Analyze complex issues and identify improvement opportunities
Requirements:
• 1+ years in clinical research (device industry strongly preferred)
• knowledge of bedside patient monitoring beneficial
• experience in systematic searches of medical/scientific literature (Embase, PubMed)
• skilled with data extraction tools (e.g., Distiller, Zotero, EndNote)
• knowledge of relevant writing styles (e.g., AMA) and good publication practices (e.g., ICMJE)
• strong knowledge of clinical research methodology (study design, outcomes, measures, biostatistics)
• strong ability to identify, mitigate, and escalate risks
• ability to prioritize and meet multiple project deadlines
• excellent written and oral English communication skills
Benefits:
• PTO
• 401k (up to 7% match)
• HSA (with company contribution)
• stock purchase plan
• education reimbursement
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