Responsible for coordinating and managing clinical trials including providing all aspects of protocol management, including screening for patient eligibility, data collection and analysis, ensuring protocol compliance, adverse drug reaction reports, monitoring patient treatment and toxicities, and maintenance of accurate and complete clinical research files. Assist the regulatory department with Human subjects submissions, renewals, and safety reports. Directly communicate with assigned physicians and disease groups, including attending weekly meetings. Provide direct assistance to the Lead CRC in reviewing and verifying university research account statements, professional fee statements, and invoicing. Arrange regular meetings with the study team(s).

• Excellent verbal and written communications and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team.

• Proficiency with Microsoft Word, PowerPoint, and Windows.

• Excellent analytical and problem-solving skills.

• Ability to work effectively in a fast-paced, team-based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects.

• Ability to establish cooperative working relationships with patients, co-workers, & physicians.

• Demonstrated proficiency with medical terminology.

• Experience working with patients or study subjects.

• Ability to abstract data from medical records and transfer it to data collection forms or directly into databases.

• Employment is subject to a criminal background check and pre-employment physical.

• Must be able to work various hours, days, and locations based on business needs.

• Occasional evenings and weekends may be required.