Instructor, Clinical Trials Research Associate Program

The instructor of Clinical Trials Research Associate is primarily responsible for the planning, delivery, and evaluation of classroom instruction, and providing related services and support activities required for optimal student learning and effective educational programming. As a member of the Clinical Trials Research Associate faculty, the instructor is also accountable for assisting and supporting the program director, field coordinator and/or department dean, as needed, in meeting the instructional and curricular requirements of the program, department, and division. More specifically, and consistent with the employee’s current contract of appointment.

1. The instructor must hold a minimum of a master’s degree in either clinical research, nursing, allied health sciences, life sciences, social sciences, or another related field
2. Must have had at least three (3) years’ of recent experience as a clinical research associate/monitor or clinical data manager in a pharmaceutical company, a medical device company, or contract research organization
3. Should have at least one (1) year of experience in the training of clinical research professionals within a pharmaceutical company, a medical device company, or contract research organization
4. Must be familiar with:
• virtual clinical trials
• real-time and remote risk-based monitoring
• eTMS, CTMS, and EDC technology

1. Must have had at least three (3) years’ experience as a research site study coordinator., clinical research associate, clinical data manager, clinical safety professional, or other clinical research professional in a pharmaceutical company, medical device company, contract research organization, or research center
2. Should have at least one (1) year of experience in the training of clinical research professionals within a pharmaceutical company, medical device company, contract research organization, or research center.

Highly preferred to have current certification by a clinical research professional organization (such as the Society of Clinical Research Associates, the Association of Clinical Research Professionals, Society of Clinical Data Management, Regulatory Affairs Professionals Society, or other clinical research professional organization) or must demonstrate competency through a combination of years of industry experience and a record of participation, publications and or presentations to relevant professional organizations/societies/associations within five years of appointment to the position.