Full-Time Technical Writer
Eurofins is hiring a remote Full-Time Technical Writer. The career level for this job opening is Entry Level and is accepting Piscataway, NJ based applicants remotely. Read complete job description before applying.
Eurofins
Job Title
Posted
Career Level
Career Level
Locations Accepted
Share
Job Details
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.
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
Education and Experience:
Bachelor’s degree
At the discretion of senior management, additional experience may qualify an individual in place of a Bachelor’s degree
Schedule:
Position is fully remote, Monday-Friday 8:00am-5:00pm