This is a Full time job
- Review and develop protocols, consent forms, manuals of procedures
- Monitor clinical study timelines and project plans
- At least 10 years of solid work experience in life science or public health
This is a Full time job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Contract/Temp job
This is a Full time job
This is a Contract/Temp job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Contract/Temp job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Part time job
This is a Contract/Temp job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Full time job
This is a Full time job