Clinical Research Coordinator — Multi-Site Trials

Accel Research Sites; Massachusetts; On-site; USD 52,000 - 78,000; Full time

Job summary

Alcanza is seeking a Clinical Research Coordinator to join our Operations team in the Boston area. The CRC will support execution of studies in compliance with GCP, ICH, FDA regulations, and SOPs, while coordinating patient enrollment, visits, and data entry.

The role requires a Medical Assistant diploma or equivalent plus 1 year of clinical research experience; bilingual English/Spanish is a plus. Strong teamwork, organization, and communication are essential in this fast-paced environment.

Qualifications

• Medical Assistant diploma or equivalent and 1 year clinical research or clinical experience.
• Proficiency with basic clinical procedures (blood pressure, vitals, EKGs, phlebotomy).
• Bi-lingual English/Spanish a plus.

Responsibilities

• Screen patients for study enrollment and obtain informed consent.
• Document in source charts and enter data in EDC.
• Obtain vital signs and ECGs; perform basic lab procedures per protocol.
• Maintain study logs, supplies, and recruitment activities.
• Monitor visits and report adverse events and deviations; ensure HIPAA compliance.
• Maintain confidentiality under HIPAA guidelines and communicate effectively with team.

Skills

Bi-lingual English/Spanish

Strong organizational skills

Written and verbal communication

Interpersonal and listening skills

Multitasking ability

HIPAA/compliance awareness

Professionalism and integrity

Independent work capability

Education

Medical Assistant diploma / LPN/LVN / EMT credential OR Associate’s degree

Tools

Microsoft Office

Electronic Health Records (EHR)

Typing speed 40+ wpm

Job description

Alcanza is seeking a Clinical Research Coordinator to join our Operations team in the Boston area. The CRC will support execution of studies in compliance with GCP, ICH, FDA regulations, and SOPs, while coordinating patient enrollment, visits, and data entry.

The role requires a Medical Assistant diploma or equivalent plus 1 year of clinical research experience; bilingual English/Spanish is a plus. Strong teamwork, organization, and communication are essential in this fast-paced environment.