Vacancy has expired
Show me jobs like this one| Job Ref: | 2946 |
| Sector: | Pharmaceutical and Medical Device |
| Job Type: | Full Time |
| State: | Maryland (MD) |
| City: | Ellicott |
| Post Code: | Dec 16, 2011 |
| Job Description: |
The successful candidate will review and interpret clinical data, independently write, edit, compile and QC documents, ensure the accuracy and quality of applicable written deliverables, and ensure compliance with ethical, legal, scientific, regulatory and client standards, in the Ellicott, MD location. Role & Responsibility - Review for quality and assist in the interpreting, analyzing and presenting data from clinical studies, including tables, figures and listings - Write, review, edit and QC documents for clients including synopses, protocols, amendments, reports, narratives, investigator brochures, informed consent forms, manuscripts, clinical development plans and analysis plans, that meet scientific and regulatory standards as applicable - Writing regulatory submissions and/or relevant sections. - Ensure proper version control of all applicable documents - Assist in preparing scientific, process and capability presentations for prospective clients (Business Development, Bid Defense) and for presenting at conferences and professional meetings - Resolve issues and escalate problems as necessary Requirements Experience & Qualification |
| Post Date: | 12/17/2011 |
