Clinical Research Medical Writer
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Key Responsibilities
• Lead the production of regulatory documentation across projects
• Collaborate with technical specialists for content accuracy
• Manage projects by tracking deliverable timelines
• Participate in quality reviews for author contributions
• Support editing and proofreading of study-related documents
Requirements:
• Minimum undergraduate degree, advanced degrees preferred
• 3-5 years of related medical writing experience
• Knowledge of GCP, GDPR, and HIPAA regulations
• Proficient in EndNote/reference software for citation management
• Strong communication skills, with an ability to work diplomatically Use your medical writing talent to support vital clinical research initiatives in this resourceful position.
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