Technical Writer
Company:
Location:United States, EST, PST
Languages:English
Skills:
Project ManagementMicrosoft ExcelDocumentationCommunication SkillsAnalytical SkillsCollaborationAttention to detailOrganizational skillsWritten communicationMultitasking
Requirements:
Ability to multi-task and discern the priority of tasks based on deliverables schedule. Adept computer knowledge i.e Microsoft Suite, Snipping Tool, Adobe or equivalent software. Proficient with Microsoft Word, Excel and Outlook. Bachelor’s degree (additional experience may qualify in lieu of a degree at senior management discretion).
Responsibilities:
Generate clinical study reports for studies conducted across multiple ECRL sites. Incorporate and/or summarize aspects of clinical study protocol, case report forms, review board documentation, data, and statistical analysis into reports. Interact with Laboratory Staff, Investigators, Statisticians, Project Managers, and Quality Assurance Auditors to coordinate data assembly and revisions. Present and orient data in appropriate tables, figures, or screenshots. Write and review clinical study protocols. Coordinate communication with Laboratory Staff and Study Sponsors during protocol review. Uphold company-wide SOPs to ensure consistency and quality. Special projects as assigned by Technical Writing Manager.
