Study Coordinator

Frontage Laboratories • Chicago, IL

4d • $22 - $26 • Onsite

About The Position

The individual in this position is involved in studies that evaluate the safety and/or toxicity of various materials (e.g., pharmaceuticals, chemicals, etc.). This position demands to be an active member of the study team and work along with the Study Directors and Report Writers and report to the Team Lead of Study Coordination group. This is a full-time on-site position at our Chicago facility with no provisions for working remotely.

Requirements

• BS or equivalent in natural sciences.
• Excellent scientific writing and documentation skills.
• Ability to work independently and in a fast-paced CRO environment.

Nice To Haves

• Experience supporting Non-GLP and GLP non-clinical toxicology studies is preferred.
• Familiarity with FDA, OECD, and GLP regulatory requirements is preferred.

Responsibilities

• Generation of study protocol based on the signed study proposal
• Generation of protocol amendments, if and when needed
• Scheduling and conducting the study start meetings
• Coordinate client visits, when requested by the client
• Generating data tables from Provantis
• Collaborate with other units to support study timelines
• Interact with Study Directors and help define study priorities and schedules
• Demonstrates the ability to contribute to the success of assignments
• Performs other duties as assigned

Benefits

• 401k Employer Match with immediate vesting
• Vision Insurance
• Medical and Dental Insurance with multiple coverage options
• FSA (Medical, Dependent Care, and Commuter)
• Short Term Disability
• Long Term Disability
• Life Insurance
• Generous Paid Holidays and PTO

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level