Clinical Research Coordinator — Multisite Trials

Alcanza Clinical Research, LLC; Gilbert (AZ); On-site; USD 36,000 - 48,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401k plan with safe harbor match

Life and disability insurance

Job summary

Alcanza Clinical Research, LLC is seeking a Medical Assistant to join the Operations team at the Phoenix Medical Trials site in Gilbert, AZ. The role supports multi-site Phase I–IV studies across multiple therapeutic areas, performing screening, consents, follow-ups, data entry in EDC, vital signs, and basic lab procedures.

The position emphasizes accuracy, confidentiality, and collaboration with investigators, coordinators, and sponsors.

Qualifications

• Requires Medical Assistant diploma, LPN/LVN, EMT credential or Associate’s degree plus 1 year clinical research or clinical experience.
• Proficiency with basic clinical procedures (blood pressure, vitals, EKGs, phlebotomy, etc.).
• Bi-lingual English/Spanish is a plus.
• Strong organizational and communication skills; attention to detail.
• HIPAA compliance awareness and handling of confidential information.

Responsibilities

• Screen patients for study enrollment and obtain informed consent.
• Conduct patient follow-up visits and document in source charts.
• Enter data in EDC and respond to data queries.
• Obtain vital signs, ECGs, and basic lab procedures per protocol.
• Manage study supplies, logs, and incident reporting as needed.
• Schedule subjects for visits and reminders; assist with site initiation and meetings.

Skills

Clinical procedures

Data entry

EHR proficiency

HIPAA compliance

Communication skills

Bilingual English/Spanish

Organizational skills

Microsoft Office

Education

Medical Assistant diploma

LPN/LVN credential

EMT credential

Associate’s degree

Tools

Microsoft Office

Job description

Alcanza Clinical Research, LLC is seeking a Medical Assistant to join the Operations team at the Phoenix Medical Trials site in Gilbert, AZ. The role supports multi-site Phase I–IV studies across multiple therapeutic areas, performing screening, consents, follow-ups, data entry in EDC, vital signs, and basic lab procedures.

The position emphasizes accuracy, confidentiality, and collaboration with investigators, coordinators, and sponsors.