Clinical Research Coordinator I (Entry Level)

Education and Experience:

1. High school diploma or equivalent. 2. Fluency in Spanish and English.

Essential Skills and Abilities:

1. Excellent communication skills and proper grammar. 2. Computer literacy. 3. Strong organization with attention to detail. 4. Empathetic personality with concern for patients' needs. 5. Knowledge of Microsoft® Excel.

responsibilities:

Assist Principal Investigator, through delegated authority, with conducting clinical trials per Federal, State, and Institutional guidelines. Learn knowledge of departmental functions through reading literature, attending workshops, seminars, and conferences, and by participating in professional organizations Learn to conduct audits of research studies to check the accuracy, integrity, and consistency of research studies Learn to coordinate study-monitoring visits Learn to coordinate research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met Assist with regulatory compliance including assisting with preparing IRB materials for approval of protocol amendments, submitting Investigational New Drug (IND) Safety Working on weekends and overnight/overtime when needed Travel required Screen subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant's eligibility or exclusion. Register participants to the CTMS system Coordinate participant tests and procedures. Collect data as required by the protocol. Assures timely completion of Case Report Forms. Maintain study timelines.

Job Type:

Full-time Benefits:

Dental insurance Health insurance Life insurance Paid time off

Work Location:

In person