Elevate your clinical research career with Alcanza as a Clinical Research Coordinator. This role involves executing studies in compliance with regulations while managing patient enrollment, data entry, and communication effectively. As a Clinical Research Coordinator, you will oversee assigned clinical studies within a multi-site environment. Your expertise in Positive Clinical Practice (GCP) and understanding of FDA regulations will ensure patient safety and data integrity.

Key responsibilities include consenting patients, documenting in clinical charts, and conducting follow-up visits for optimal participant care. Key Responsibilities:

- Screen patients for study enrollment
- Document patient interviews and consent processes




- Enter data accurately in Electronic Data Capture (EDC)
- Schedule and remind subjects for study visits
- Conduct monitoring visits and manage related issues Requirements:
- 3+ years as a Clinical Research Coordinator
- Medical Assistant diploma or equivalent experience
- Proficiency in basic clinical procedures
- Strong organizational and communication skills
- Ability to travel up to 100% of the time Bring your clinical skills, attention to detail, and commitment to patient care to advance vital research at Alcanza.

📌 Clinical Research Coordinator at Alcanza (Burlington)
🏢 ActivMed Practices u0026 Research
📍 Burlington