Clinical Research Coordinator I

Responsibilities

• Screen and enroll clinical research study subjects following established SOPs and GCP guidelines
• Obtain informed consent and ensure all patient privacy and safety protocols are met
• Perform basic clinical procedures including blood draws (phlebotomy), vital signs, and ECGs
• Review laboratory, ECG, and other test results for completeness and alert values
• Maintain accurate documentation, including real-time data entry and study medication inventory
• Identify and promptly report adverse events (AEs) and serious adverse events (SAEs)
• Assist with patient recruitment efforts and the creation of recruitment materials
• Coordinate with clinical staff and Sponsor/CRO representatives during site visits

Requirements

• Minimum of 1 year of experience as a Clinical Research Coordinator
• Recent phlebotomy experience is required
• Strong knowledge of Good Clinical Practices (GCP) and federal research regulations
• Proficiency in MS Word and Excel
• Ability to work onsite 5 days per week in Mesa, Arizona

Preferred Qualifications

• Bachelor's Degree in a related field
• Excellent working knowledge of medical and research terminology
• Strong organizational, prioritization, and attention to detail skills

Benefits

• 100% employer-paid medical, dental, and vision insurance options
• Paid Time Off (PTO) and company-paid holidays
• 401(k) retirement plan with company match
• Health Savings Account (HSA) and Flexible Spending Accounts (FSA)
• Company-paid short-term and long-term disability insurance

About the Company

Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow.