Clinical Research Coordinator – Join Our Growing Team!

The CRC is responsible for managing and conducting clinical research projects by leading overall trial operations, collecting data, informing study participants about study objectives, administering questionnaires, ensuring US Foot and Ankle Specialists Standard Operating Procedures (SOPs) are followed and working closely with the sponsor/Clinical Research Organization (CRO).

Clinical Research Coordinator Essential Functions/Responsibilities (other duties may be assigned): 

• Oversee daily clinical trial operations and ensure compliance with study protocols
• Screen and enroll participants, obtain informed consent, and collect study data
• Coordinate with investigators, sponsors, and research staff
• Maintain accurate study records and regulatory documentation
• Manage inventory, lab work, and study supplies
• Be a point of contact for participants throughout the trial

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Clinical Research Coordinator Required Education, Skills and Experience: 

• 2+ years of clinical research coordination experience preferred
• Associate’s degree in health sciences, biology, or related field (or equivalent experience)
• Excellent organizational skills, attention to detail, and ability to multitask
• Strong communication skills – you’ll be working with patients, providers, and sponsors
• Willingness to travel between Louisville, Shepherdsville & Shelbyville

Why You’ll Love Working Here:

• Health, life, and disability insurance
• 401(k) with company match
• PTO + paid holidays
• Employee discounts
• A supportive and collaborative work environment

Physical Requirements: 

• Ability to sit, stand, and perform clinical tasks as needed
• Lift up to 50 lbs occasionally