Job Summary:

The Clinical Research Associate I (CRA I) will have a detailed understanding of each study protocol and background knowledge of the study medication and therapeutic area under study; determine subject population availability and list and clarify concerns with the Principal Investigator (e.g. inclusion/exclusion criteria, concomitant medications, medical history, baseline imaging requirements).Duties include but are not limited to: understand the requirements and objectives of each clinical protocol; research questions regarding protocol or eligibility for physicians or support staff; respond to requests from sponsors regarding patient data; independent development and execution of all aspects of protocols; coordination of early and late phase trials in investigator-initiated, NCI sponsored, and industry trials; compliance assurance with federal guidelines. The CRA I will be expected to follow patient course of treatment by ensuring all procedures are being conducted per protocol, collecting appropriate data from medical records; distribute and collect specified survey instruments; monitoring patients closely for any associated adverse events, maintain clinical research records; maintain files of approval letters and annual review reports; maintain records of closed protocols for physician use/queries on patients; distribute protocols and updates to appropriate personnel. 

Minimum Qualifications:

Bachelor's degree and two years related experience or equivalent combination of education and experience. Working knowledge of medical terminology, basic computer skills and excellent written/oral communication and organizational skills.

Preferred Qualifications:

Certified Clinical Research Professional (CCRP) certification.

Work Days:

Monday to Friday 8 am - 4:30 pm

Message to Applicants:

Salary Range-$62,354-$68,000

Recruitment Office: Human Resources