Benefits:

401(k)

401(k) matching

Dental insurance

Health insurance

Paid time off

Job description

We are looking for candidates in Huntsville, AL with a medical background and excellent interpersonal experience to support, facilitate, and organize daily human clinical trial activities. This person will be an integral part of the research team and play a part in the day-to-day running of human trials.

The following are a list of responsibilities:

—experience with standard regulatory submissions (including 1572 and IRB)

—review and execute trial activities as outlined in the study protocol

—direct and participate in protocol training for research staff

—obtain informed consent from potential subjects

—write SOPs and update source documents as needed

—organize subject binders

—have a working knowledge of sponsor/FDA audits

—GCP certified

—previous clinical trial experience

—computer skills are essential (incl. Excel, Adobe, Word, etc)

—familiar with device skills including study devices, pt devices, iPhones, etc.

—act as the liaison between regulatory authorities and the research team

—other duties as needed

Personal Characteristics

—honest, high integrity a must

—highly organized, detail-oriented, meticulous and thorough

—life learner

—able to handle increased amounts of paperwork

—compassionate and caring

—able to work independently

—self-motivator

**Salary based on experience. Benefits available if needed.