Description
Major responsibilities include:- Obtain and maintain essential documentation in compliance with ICH-GCP, as well as other procedural documents and local regulations.
- Contribute to the selection of potential investigators.
- Design draft budget for designated studies.
- Update IMPACT and other systems with data from centres in a timely matter.
Looking for a passionate individual who is able to communicate with senior figures. Site start up is a plus.
Therapeutic areas: Oncology, Respiratory and Cardiovascular.
Rate: $40-50/hr
Duration: 1 year (possible extension for up to 3)
Location: Wilmington
If this sounds like an opportunity that you are interested please reach out with an updated copy of your resume as well as your contact information.
If you know someone who may be a better fit, please feel free to pass along their information.
Turnaround for these roles will be very quick.