Job DutiesJob Qualifications Job Duties Responsibilities
Under direction of the lead study coordinators, the Study Coordinator Assistant will be involved with various research studies and one clinical trial.
The roles of this position are to provide administrative support for several research studies, maintain IRB documentation, coordinate records keeping and sample management, act as liaison with the study participants and laboratory, enter data and maintain study databases, assist the study physicians in study-
related medical procedures, and draft study-related correspondence.
Job Qualifications Qualifications
Knowledge of basic clinical and scientific terminology.
Prior study in biological sciences, or experience in a physician’s office or other clinical setting.
Skill in communicating, orally and in writing, concise clinical patient data in appropriate medical terminology at levels accessible by (1) physicians and (2) laypersons.
Proficiency in PC-based software applications, including word processing, spreadsheets and clinical database management.
Skill in composing concise, logical and grammatically correct business reports and correspondence.
Ability to establish and maintain cooperative, honest and respectful professional relationships with staff, faculty, fellows, patients and patient families, as well as with personnel at all levels of the organization.
Excellent English-speaking, reading and writing capability.