BS degree in Life Sciences, Healthcare Management, Nursing or a related field or equivalent work experience
Minimum 1-3 years' experience working in a similar capacity.
Must be bi-lingual in Spanish (written and oral)
Proficiency with MS Office Suite, particularly Word and Excel
Working knowledge of clinical research process – i.e. budgeting, participant recruitment, protocols, consenting process, records and regulatory management requirements, etc.
Working knowledge of medical terminology
Possess superior organization skills – data and document management
Knowledge of good clinical practices and patient assessment
Effective interpersonal skills – ability to be firm, yet diplomatic
Ability to work well under pressure and meet multiple and sometimes conflicting deadlines
Description of Duties:
Management of clinical trials: patient recruitment; coordination and monitoring of study visits and study procedures; venipuncture, breast milk collection, assessment of infants, data collection, patient education, investigator meeting participation
Research study protocols - understanding inclusion/exclusion criteria, understanding medical diagnostic tests
Oversight of clinical and research activities in the clinic