Employment Type : Full-Time
SUMMARY The Recruitment Coordinator assists clinical research coordinators and investigators in the recruitment of study participants for Phase I, II, III, IV, clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols. DUTIES The Recruitment Coordinator has partial responsibility for these areas: SUPERVISION Work is performed under general supervision from the principal investigator or Site Director/Manager. SKILLS/QUALIFICATIONS Position requires at minimum an associate’s degree in a biomedical field, business, or equivalent combination of post secondary education, medical certification, medical licensure, and/or at minimum 2 years healthcare experience. MUST be bilingual in the English and Spanish language. EQUIPMENT Must be familiar with medical terminology used in the Clinical Research Site. WORKING CONDITIONS Work is performed in an office environment. The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. Management retains the right to add or to change the duties of the position at any time. Job Type: Full-time Pay: $13.00 - $16.00 per hour Benefits: Schedule: Experience: Language: Work Remotely: