What are the responsibilities and job description for the Clinical Trials Research Coordinator position at Rose International?
Education required : High School Diploma or General Education Development (GED) required.
Education preferred : Associates degree or higher OR 2 years of work experience in an ambulatory and / or acute health care setting required (LVN maybe substituted for an Associates degree)
Qualifications :
- Clinical trials experience preferred.
- Phlebotomy and / or medical assistant certification preferred but not required
The Clinical Trial Research Coordinator I (CTRC-I) is a novice level position which, under the clinical direction of the Principal Investigator (PI), assists in the operational and administrative research support of the Client Northern California (Client) PI and Client Clinical Trials Operations Director or designee, and other research staff conducting multiple FDA-regulated clinical trials. This is a non-licensed position which works under the daily supervision of an experienced Clinical Trial Nurse, Clinical Trial Research Coordinator, and / or KFRI-designated, licensed clinical trial research staff member. This position must adhere to the positions scope of practice as outlined in the Major Responsibilities below. This position is also responsible for assisting in protecting the health, safety, and welfare of research participants.
Work Days : Scheduled days and hours are contingent upon departmental needs. Normal schedule : M-F (8 : 00am – 5 : 00pm).
Additional Requirements :
