Clinical Research Coordinator jobs in Paramus, NJ

We are seeking a Per Diem Clinical Assistant II for our growing organization!

Responsibilities include, but are not limited to:

• Tracks and maintains an inventory of supplies in study exam rooms

• Reads, understands, and follows Standard Operation Procedures

• Executes tasks with good understanding of proper technique, SOP’s, and GCP’s

• Able to understand general study exclusionary criteria (cancer restrictions, medication use, etc.)

• Utilizes specialized computer software (SMS, RMS, Enrollment Log, etc.) to update study files

• Performs miscellaneous clinical and non-clinical duties upon request, as needed

Minimum High school diploma, but bachelor’s degree preferred. Minimum 2 years relevant work experience in clinical research or health related environment. Strong clinical skillset is required (blood draws, EKGs, vitals). Ability to follow general guidance and direction in accordance with FDA regulations and GCP/ICH guidelines as they apply to the conduct of clinical research. Strong interpersonal, written and verbal communication skills are required. Able to read, understand and build knowledge of study instructions, protocols and procedures. Ability to convey courtesy and empathy for subjects/patients. Excellent organizational skills. Attention to detail. Consistency in meeting deadlines. Familiarity and comfort in learning Microsoft Office Suite and related application software. Able to work assigned study schedules, as determined by clinical study demands and TKL business needs and priorities. This is a per diem position based primarily in our Fair Lawn, NJ office. Shifts typically run from 7pm-11pm, 11pm-7am, or 7pm-7am. Primary need is Friday, Saturday, and Sunday nights.