Job Abstract

As the Senior Clinical Research Coordinator you will be primarily responsible for the coordination of research activities under the direct supervision of the Westwood Translational Clinical Team Manager. You will be responsible for ensuring protocol procedures are completed accurately, safely, and in a timely manner. This includes responsibility for research assessment and patient intervention under the supervision of the Principal Investigator. Additional responsibilities may include:

• Regulatory compliance

• Patient recruitment and enrollment

• Data collection

• Research chart documentation

• Quality assurance

• Report preparation

• Protocol information dissemination

• Sample management

• Budget reviews

You will also meet with staff on an annual basis to develop and implement career goals in order to encourage and promote professional growth and development. Travel to other locations may be required.

Salary Range: $80,304.48 - $129,184.56/year

Required:

• Bachelor’s Degree or three-to seven years of study coordination or clinical research coordination experience

• Ability to work in more than one environment, travel to participating hospitals/sites, and attend off site staff meetings, conferences and investigator meetings.

• Advanced knowledge of Good Clinical Practice (GCP) for clinical research.

• Advanced typing and computer skill/ability including word-processing, use of spreadsheets, email and data entry

• Ability to work efficiently and complete tasks with a high degree of accuracy.

• Demonstrated organizational skills to handle multiple clinical research projects for efficiency and cost-effectiveness, including handling work delegated by more than one individual.

• Ability to work flexible hours to accommodate research procedures and deadlines.

• Demonstrated computer skills using Word, Excel, PowerPoint, Outlook, e-mail and databases to create reports, correspondence and other documents as required.