Technical Writer

Primary Duties and Responsibilities:Generate clinical study reports for studies conducted across multiple ECRL sites;Incorporate and/or summarize aspects of the clinical study protocol, case report forms, review board documentation, data generated during the study, and statistical analysis into clinical study reports;Interact with Laboratory Staff, Investigators, Statisticians, Project Managers and Quality Assurance Auditors from any or all of the ECRL sites to coordinate the assembly of data, documentation, methodology, and necessary revisions to clinical study reports;Present and orient data in appropriate tables, figures or screenshots;Write and review clinical study protocols, incorporating specifications of Investigators, Laboratory Staff, Statisticians and Study Sponsors;Coordinate communication with the Laboratory Staff and Study Sponsors during the review of the clinical study protocol;Uphold company-wide SOPs to ensure consistency and quality throughout protocols and reports;Special projects as assigned by Technical Writing Manager.