Clinical Trial Assistant

The Steely Group; Skokie (IL); On-site; USD 48,216 - 55,104; Part time

Benefits offered by this job

Medical insurance

Vision insurance

Job summary

A biotechnology firm in Skokie, IL is seeking a Clinical Trial Assistant to support clinical research activities. The ideal candidate will have 2-4 years of relevant experience in biotech and possess excellent communication and organizational skills. This role includes responsibilities such as document management and ensuring adherence to regulations.

Qualifications

• 2-4 years relevant CTA experience, ideally in biotech.

Responsibilities

• Supporting clinical research activities.
• Collecting and archiving information and documents.
• Ensuring complete and correct study administration.

Skills

Excellent communication

Organizational skills

Job description

This range is provided by The Steely Group. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$35.00/hr - $40.00/hr

Direct message the job poster from The Steely Group

The Clinical Trial Assistant is responsible for supporting clinical research and development tasks. The CTA will work closely with the Clinical Operations team, which is responsible for monitor planning and executing clinical trials.

You have an important task in study start-up, digital sending, tracing and administration as well as saving essential documents (e.g., case report forms, CVs, study protocols, investigator brochures, informed consent forms and study supplies), and filing important records related to side effects.

Clinical Trial Assistant roles and responsibilities cover a range of tasks in support of a clinical study, including:

• collecting, registering and archiving information and documents in accordance with the applicable good clinical practice guidelines for clinical studies;
• preparing investigator site files, trial master files (TMF) and electronic trial master files (eTMF) for the initiation of participating centers in clinical studies;
• identifying needs, bottlenecks and deviations within your own study team;
• participating in projects or initiatives on request, or on your own initiative;
• taking on department-wide tasks to contribute to the optimization of processes within the department;
• maintaining the complete documentation for the studies assigned;
• ensuring complete and correct study administration in accordance with the standard operating procedures and the ICH-GCP guidelines;
• submission of clinical trial documents for review and approval

Requirements:

• 2-4 years relevant CTA experience, ideally in biotech
• Excellent communication and organizational skills

Seniority level

• Associate

Employment type

• Contract

Job function

• Research
• Industries: Biotechnology Research and Pharmaceutical Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

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