Highlights:

• Growing Company: Join a rapidly expanding team at ReHealth, a global leader in clinical trials for cognitive impairment.
• Hybrid Role: Flexible working with a combination of remote and in-office work based in Chicago, IL.
• Professional Development: Continuous learning opportunities and career growth.
• Comprehensive Benefits: Excellent health, dental, vision insurance, 401(k) with employer match, PTO, and more.

About the Role:

Our client is seeking a dedicated Clinical Trials Start-Up Coordinator to join their clinical trials team. This role involves managing the start-up process for clinical trials across all site locations in the US, ensuring compliance with ICH GCP guidelines and trial-specific protocols.

Key Responsibilities:

• Manage the clinical trials pipeline tracker and report on progress.
• Complete and submit site-specific feasibility and pre-qualification processes.
• Coordinate set-up activities and prepare essential documentation.
• Ensure preparation and amendments of site-specific Informed Consent Forms (ICF).
• Collaborate with third-party vendors, CROs, and sponsor representatives.

Requirements:

• Bachelor's degree in a science, technical, or health-related field.
• Minimum 1 year of experience in clinical research at site level.
• IT proficiency, HIPAA, and GCP trained.
• Excellent verbal and written communication skills.
• 6 months of experience in CNS trials is preferred
• Experience with electronic data capture systems, e.g., Medidata RAVE.

Benefits:

• 4 weeks PTO
• Health, dental, and vision insurance
• 401(k) retirement plan with employer match
• Life and disability insurance
• Health Savings Account
• Professional development assistance