Clinical Trial Operations Specialist

Cellectis; New York (NY); On-site; USD 80,000 - 90,000; Full time

Job summary

A biotechnology company located in New York is seeking a Clinical Trial Associate to support clinical study teams in the execution and oversight of clinical trials. The role involves managing key documentation, ensuring compliance with regulatory standards, and tracking the progress of clinical studies. Candidates should possess a Bachelor’s degree and 1-3 years of experience in clinical trials, with knowledge of FDA regulations and strong organizational skills. The compensation range is competitive, between $80,000 and $90,000.

Qualifications

• Minimum of 1–3 years of experience supporting clinical trials.
• Experience in a pharmaceutical, biotechnology, or CRO environment preferred.

Responsibilities

• Support study start-up activities, including site feasibility and regulatory document collection.
• Maintain inspection-ready Trial Master Files.
• Track study progress and generate routine status reports.
• Coordinate internal and external study meetings.

Skills

Foundational knowledge of FDA and/or EMA regulations

GCP requirements

Strong attention to detail

Organizational skills

Proficiency in Microsoft Office applications

Education

Bachelor’s degree (BS/BA) or equivalent

Tools

eTMF

CTMS

EDC platforms

Job description

A biotechnology company located in New York is seeking a Clinical Trial Associate to support clinical study teams in the execution and oversight of clinical trials. The role involves managing key documentation, ensuring compliance with regulatory standards, and tracking the progress of clinical studies. Candidates should possess a Bachelor’s degree and 1-3 years of experience in clinical trials, with knowledge of FDA regulations and strong organizational skills. The compensation range is competitive, between $80,000 and $90,000.