Research Associate - Contract Assignment

Clincial Research Associate

Job Purpose:

Supports clinical trials by planning, collecting, screening, and summarizing information gathered.

Duties:

* Plans information acquisition by identifying potential investigators, conducting pre-trial site visits, training site staff; monitoring trial drug accountability; studying clinical requirements; evaluating resources.

* Collects information by searching and interviewing patients; comparing information discovered to information specifications; preparing correspondence.

* Screens information by tracking patient enrollment and status.

* Prepares research reports by confirming Case Report Form (CRF) and Severe Adverse Event (SAE) reporting; identifying protocol deviation; summarizing information; citing patient response; adhering to federal guidelines.

* Protects organization's value by keeping research information confidential.

* Updates job knowledge by participating in educational opportunities; reading technical and professional publications.

* Enhances research and organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.

Skills/Qualifications:

Reporting Skills, Bioinformatics, GCP, Clinical Research, Analyzing Information, Research Skills, Confidentiality, Nursing Skills, Teamwork, Verbal Communication, Problem Solving

Send resume to: tfoster@odcpharma.com