Coordinate all aspects of clinical research trials, ensure compliance with protocols, ensure regulatory compliance, liaison with monitors and sponsors, schedule

Hours for part time will be discussed during interview. You will essentially take a patient from scheduling all the way through their insurance verification,

Bachelors Degree or foreign equivalent in related field or equivalent experience. 6+ years of object-oriented analysis and design.

Assist with incoming and outgoing mail correspondence. Keep reception area clean and welcoming. Administrative or clerical experience a plus.

Knowledge of and/or technical experience in English, journalism, public relations, photography, video and graphic design/desktop publishing preferred.