Job Description:
- Pay: $45-50/hr.
- Travel: 30-50%
- 6-month assignment with possibility for extension or conversion based on performance and budget.
- Responsible for conducting Phase I-IV studies per Federal Regulations and ICH guidelines.
- Write study protocols, monitor site adherence, ensure timely patient enrollment, and manage CRF processing and data cleanup.
- Assist senior staff with study planning, designing CRFs, managing CROs, training investigators, and preparing submissions.
Qualifications:
- Bachelor’s Degree with 3+ years of experience at the CRA or CRC level is Required.
- Experience with site monitoring on the sponsor side is Required.
- Experience with medical device or in-vitro device study is Required.
If you are interested in hearing more about the position, please respond to this posting with your resume attached or contact me at 813-302-1679. Please forward this email to any friends or colleagues as we do offer a Referral Bonus for any candidate who is hired and still gainfully employed after 30 days.
Who We Are:
The Fountain Group is a nationwide staffing firm with over 80 Fortune 100-500 clients. Since 2001, TFG has maintained a consistent standard of excellence, and our work is broadly recognized every year through numerous industry performance awards. Our success is a team effort. Browse our website below for additional information on our company. The Fountain Group
“We work in Life Sciences, Clinical, Engineering, IT, and more. Above all, we specialize in people.”