Clinical Trial Assistant — Grow in Biotech with Benefits

SystImmune, Inc.; Princeton (NJ); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Insurance coverage

401(k) with company match

Paid time off

Holidays

Job summary

SystImmune, Inc. in Princeton, NJ is seeking a Clinical Trial Assistant to support day‑to‑day operations of clinical studies, ensuring compliance with ICH GCP and SOPs. You will help with documentation, meetings, and cross‑functional communications.

The role involves study start‑up activities, TMF maintenance, site coordination, and tracking recruitment, visits and audit readiness. A Bachelor’s degree and 2 years’ research experience are preferred.

Qualifications

• Bachelor’s degree in health science or related field is required.
• 2 years in research experience preferred.
• Excellent verbal and written communication skills required.
• Excellent organizational, multi-tasking and time management skills required.
• Located in NJ or can commute to Princeton, NJ.

Responsibilities

• Develop and distribute meeting agendas, minutes and monthly status reports to document key project updates and communications to relevant stakeholders.
• Participate in regular team meetings, CRO, Vendor and Investigator Site meetings as necessary.
• Support Clinical Project Management team in communication to CRO, Vendors and Investigator Sites.
• Support study start-up activities, including preparing/reviewing study-related documents.
• Assist in tracking subject recruitment, monitoring visits, and protocol deviations.

Skills

Communication

Organizational skills

Travel flexibility

MS Office

CTMS/EDC/eTMF familiarity

GCP knowledge

Education

Bachelor’s degree in health science or related field

Tools

CTMS

EDC

eTMF

SharePoint

Teams

Word

Excel

PowerPoint

Job description

SystImmune, Inc. in Princeton, NJ is seeking a Clinical Trial Assistant to support day‑to‑day operations of clinical studies, ensuring compliance with ICH GCP and SOPs. You will help with documentation, meetings, and cross‑functional communications.

The role involves study start‑up activities, TMF maintenance, site coordination, and tracking recruitment, visits and audit readiness. A Bachelor’s degree and 2 years’ research experience are preferred.