Preclinical Study Specialist 1

Veranex, Inc. • Atlanta, GA

12d • Hybrid

About The Position

Veranex’s mission as an Innovation CRO is to improve patient outcomes by accelerating our clients’ innovations to market. As the world’s only end-to-end professional services firm focused on MedTech, we take clients’ Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.
About This Role
The Preclinical Study Specialist I supports the execution of preclinical studies, including in vivo and procedural work, data collection, and study documentation. This role plays a critical part in ensuring studies are conducted in compliance with Good Laboratory Practice (GLP) regulations and internal procedures.

Requirements

• Bachelor’s degree in life sciences or related field
• 0–3 years of relevant experience in research, laboratory, or preclinical environment
• Strong attention to detail and organizational skills
• Ability to work in a fast-paced, team-oriented environment
• Willingness to work in an in vivo research and operating room setting

Nice To Haves

• Experience in preclinical research or CRO environment
• Exposure to GLP or regulated studies
• Experience with biological sample handling and documentation

Responsibilities

• Support in-life study execution, including operating room procedures and data collection
• Accurately record raw data and observations in compliance with GLP requirements
• Assist with sample collection, processing, tracking, and shipment
• Maintain study documentation and regulatory files
• Identify and escalate deviations or issues impacting study integrity
• Collaborate with Study Directors, veterinary staff, and cross-functional teams
• Ensure adherence to study protocols, SOPs, and regulatory standards

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 251-500 employees