Teach all courses as assigned, for the full duration of scheduled instruction;
Be fully prepared with course syllabus and instructional plans for each class session in accordance with the stated objectives of the course;
Enforce academic policies and procedures of the College and the department at all times, and complying with all other institutional rules and regulations pertinent to classroom instruction and general employment;
Be available during posted out-of-class hours to students requiring additional assistance;
Contribute to the development, implementation and evaluation of competency-based education and utilize available educational resources for the evaluation, improvement of instruction and the development of teaching materials;
Take advantage of in-service training and other opportunities for continued professional development, including attendance at off¬-campus activities, as feasible, and generally staying abreast of developments in the field of instruction;
As appropriate or as requested to participate in the program, departmental, divisional, and instructional meetings and other announced activities;
Assume other necessary responsibilities and perform additional tasks as assigned by the program director and/or department dean in meeting the needs of the program, department, division, and the College.
The instructor (part-time) of Clinical Trials Research Associate or Medical Product Safety/Pharmacovigilance 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 Health Technologies faculty, the instructor is also accountable for assisting and supporting their assigned program director, field coordinator and/or department dean, as needed, in meeting the instructional and curricular requirements of their program, department, and division.
1.The instructor must have a minimum of a baccalaureate degree in biology, health sciences, or allied health. 2.The instructor must also have at least three (3) years' experience as a clinical research professional working in the pharmaceutical industry, the medical device industry, and major contract research organization or research center. 3.Must be an active member of SoCRA (Society of Clinical Research Associates) or ACRP (Association of Clinical Research Professionals) or SCDM (Society of Clinical Data Management or any other appropriate industry-recognized professional association/society.