PROJECT DETAILS:
Experienced Medical writer needed to prepare, collect and write multiple modules of an NDA as well as contribute to the creation
of several clinical study reports. QCing tables as well and using an document control system for version control. The NDA filing will be on
a rapid schedule.
REQUIREMENTS:
Experience putting together and writing modules of an NDA.
In addition, the writer must have written CSRs before in a clinical/pharmaceutical environment.
SCOPE:
The project will be for 2 months. (However, we will write the contract into December to insure that any follow up is covered)
The writer must be open to working more than 40 hours a week- some weeks more.
It can mostly be done offsite but would require an onsite presence in Boston area at times.
Compensation: commensurate with experience
This is a contract job.
Principals only. Recruiters, please dont contact this job poster.
Please, no phone calls about this job!
Please do not contact job poster about other services, products or commercial interests.
