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.
Qualifications :
- 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:
- Bachelors degree
- At the discretion of senior management additional experience may qualify an individual in place of a Bachelors degree
Additional Information :
Schedule:
- Position is fully remote Monday-Friday 8:00am-5:00pm
What we offer:
- Excellent full time benefits including comprehensive medical coverage dental and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Eurofins USA Consumer Product Testing is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
Yes
Employment Type :
Full-time