Clinical Research Associate

Responsibilities

• Conduct routine and complex monitoring visits to ensure study compliance with protocols, regulatory requirements, and GCP standards
• Manage site performance by reviewing enrollment progress, data accuracy, and protocol adherence across multiple studies
• Act as a key point of contact for investigative sites, providing ongoing support and resolving study-related issues
• Evaluate clinical data and documentation to ensure patient safety and data integrity throughout the trial lifecycle
• Collaborate with cross-functional teams and sponsors to drive study milestones and maintain timelines

Requirements

• 3+ years of CRA experience with strong exposure to Cardiovascular, CNS, Diabetes, and GLP-1 trials
• Demonstrated ability to independently monitor studies and manage multiple sites simultaneously
• In-depth knowledge of ICH-GCP guidelines, FDA regulations, and clinical trial processes
• Prior experience working directly with sponsors or CROs in a fast-paced environment
• Able to travel approximately 25–40% as needed

Compensation

$100,000 – $125,000 annually

Benefits

• Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.
• Remote work flexibility with travel reimbursement