Project Specialist II TCRA (Trial Ops Clinical Research Assoc.)

A global leader in Medical Devices is looking for a contract CRA onsite in Minneapolis. The position is for a Project specialist and is expected to look after various aspects of the trial operations as a clinical research associate. The contract is expected to last 6 months.

This is an opportunity to break into the pharmaceutical and medical device industries clinical operations niche and play an integral role in the development of the safety and efficacy of life saving devices.

Key Responsibilities:

1. Review site ICF (Informed Consent Form)

2. Review and work within Budget and Timeline

3. Process critical study documents.

4. Participate in Site Selection

5. Support multiple studies simultaneously

6. Communicate professionally verbally and in writing

7. Ensure all regulatory requirements are followed

8. Minimal QC work required

Qualifications:

1. 2-4 year degree preferred focusing in human clinical study

2. Experience with Study Start-Up

3. Experience with CTMS is a plus

4. Must have experience following SOPs

To find out more about Real Staffing please visit www.realstaffing.com