Oncology CRA Jobs

Now hiring for various positions across the United States

Job Description
Performs and coordinates all aspects of the clinical monitoring process in accordance with GCPs and global SOPs and study protocols. Conducts site visits to determine protocol and regulatory compliance, and prepares required documentation. Responsible for multiple projects and must work both independently and in a team environment. May participate in the study development and start up process including reviewing protocols, designing and/or reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings, and working with management on monitoring strategy.

Qualifications
BS/BA with experience in oncology clinical research, with two years of on-site clinical monitoring experience. This position requires excellent verbal and written communication skills. In addition, excellent interpersonal skills with strong organizational skills with attention to detail is needed. Must be computer literate and proficient in MS office. Must be able to travel depending on project needs.

How to apply