Full-time or Part-time position for a Study coordinator for a busy Beverly Hills speciality pediatric practice. The ideal candidate should be well organized and have excellent communication skills, as well as having experience in pediatric clinical trials.
Summary of Essential Job Duties:
1. Recruit and select potential study participants (young people ages 10-17 years) and obtain clinical information from patients.
2. Assist PI with assurance of FDA/NIH compliance regulations and good clinical practices for study site. This includes preparation of study application packets, including consent forms, all critical study related documents (FDA forms, radiation safety, pharmacy, etc) and submit to the IRB. Assist in preparing and submitting all amendments, updates, continuing reviews, adverse events, reports and other modifications as required by regulations and the study itself.
3. Assist PI in conducting clinical trials, including selection of patients, obtaining informed consent, administering study medication, obtaining and shipping samples, keeping CRFs up to date, maintaining records, and responding to queries in a timely manner.
Nursing or medical background preferred. BA/BS required. One-two years minimum experience in a medical or research environment.
Other requirements include:
Familiarity with medical terminology
Proficiency in Windows and MS Office
Certification in GCP and Phlebotomy
Bilingual with Spanish speaking a MUST
Contacts in the Greater Los Angeles medical community highly desirable.
Professional references required