Clinical Trials Analyst I - Remote

Overview

The Clinical Trial Analyst I is responsible for reviewing medical charts to prescreen and refer clinical research study subjects, as well as entering clinical trial data using GRN technology.

In Short

• Review medical records to determine patient eligibility for clinical studies.
• Maintain a watch list for future patient eligibility.
• Communicate eligibility and logistical information to clinical research staff.
• Provide feedback on technology-enabled patient lists.
• Collaborate with management and site staff to interpret medical records.
• Enter protocol-required information into study databases.
• Track progress in study applications and communicate with Project Managers.

Requirements

• BA/BS degree preferred or equivalent experience.
• Understanding of clinical research fundamentals.
• Basic knowledge of SOPs, FDA regulations, and ICH GCP guidelines.
• One year of experience in nursing, public health, clinical research, or health administration.
• Strong communication and organizational skills.
• Proficiency in MS Word and Excel.
• Ability to learn new software quickly.

Benefits

• Work in a corporate or home office environment.
• Standard working hours (8AM – 5 PM).