Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.
Job Description
Clinical Trial Associate iCTS Holdings LLC Fort Lee, NJ Job Details Full-time | Contract $25 - $35 an hour 11 hours ago Qualifications Spanish High school diploma or GED Medical administrative support Attention to detail Organizational skills Productivity software
Full Job Description Job Description:
The Clinical Trial Assistant (CTA) plays a key supportive role in the day-to-day operations of clinical research studies conducted at various sites linked with iCTS. Working under the supervision of the Principal Investigator and Clinical Research Coordinator, the CTA helps ensure clinical trials are conducted in compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP).
Key Responsibilities:
Assist with study start-up activities, including regulatory submissions and document collection. Maintain and organize essential clinical trial documents (e.g., investigator site files, regulatory binders). Schedule and confirm participant visits and procedures. Support data entry and query resolution using electronic data capture (EDC) systems. Assist with the preparation for monitoring visits, audits, and inspections. Communicate with sponsors, CROs, and study participants as needed. Ensure accurate filing and archiving of study-related documents. Perform other administrative tasks to support the clinical research team.
Qualifications:
High school diploma or equivalent (Associate's or Bachelor's degree in a health-related field preferred). Prior experience in a clinical research setting is an asset but not required. Strong organizational skills and attention to detail. Proficient in Microsoft Office and comfortable learning new software. Good interpersonal and communication skills. Ability to handle multiple tasks and in a fast-paced environment. Looking for a Spanish speaker