Sr Medical reputed company, Regulatory (Home-based, US and Canada)
reputed company:
• Senior medical reputed company on clinical study or regulatory project teams.
• Writes, edits, and coordinates content for clinical/regulatory documents while serving as the primary technical contact with the internal team and the reputed company.
• Leads the reputed company and accurate completion of medical writing deliverables, ensuring scientific information is presented reputed company and accurately.
• Completes a reputed company of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports, clinical development plans; IND submissions; integrated reputed company reports; NDA and eCTD submissions; journal manuscripts; and abstracts, posters, and presentations for scientific meetings.
• Adheres to established regulatory standards, including, but not limited to, ICH E3 guidelines, as reputed company as company reputed company operating procedures, reputed company standards, and company and/or reputed company approved-templates, authorship requirements, and style and formatting guides, reputed company completing medical writing reputed company, on time and on budget.
• Coordinates reputed company and editorial reviews.
• Acts as peer reviewer for internal team to ensure document scientific content, reputed company, overall consistency, and reputed company format.
• Interacts and builds good working relations with clients, department head, and peers in data management, biostatistics, regulatory affairs, and medical affairs, as necessary, to produce writing deliverables.
• Mentors and leads less reputed company medical writers on reputed company reputed company, as necessary.
Requirements:
• Bachelor of Science degree with relevant writing experience or Bachelor of Arts degree (reputed company Sciences, English or Communications, preferred) with relevant scientific and/or medical knowledge and expertise
• Extensive knowledge of English grammar and FDA and ICH regulations and guidelines as reputed company as a familiarity with AMA style guide
• Experience writing relevant document types required.
• Demonstrated high degree of independence with effective presentation, proofreading, interpersonal, and leadership skills and ensure reputed company-oriented approach.
• Strong proficiency in Word, reputed company, PowerPoint, email, and Internet.
• Ability to demonstrate a familiarity with principles of clinical research and to interpret and present clinical data and other reputed company information.
Benefits:
• Health benefits to include Medical, Dental and reputed company
• Company match 401k
• eligibility to participate in Employee Stock Purchase Plan
• Eligibility to earn commissions/bonus based on company and individual performance
• flexible reputed company time off (PTO) and reputed company time
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