Clinical Research Coordinator

Alliance for Multispecialty Research LLC; Tempe (AZ); On-site; USD 36,000 - 48,000; Full time

Job summary

Alliance for Multispecialty Research LLC in Tempe, AZ is seeking a Research Assistant to perform a wide range of administrative and clinical tasks to support study sites. You will assist with protocol adherence, data collection, patient interactions, and study logistics to ensure accurate study execution and audit readiness.

The role emphasizes compliance with GCP, FDA regulations, and sponsor requirements, with potential weekend/overtime hours as needed to support study activities.

Qualifications

• Medical office experience or equivalent work experience.
• Phlebotomy skills preferred.
• Excellent attention to detail.
• Strong listening, verbal and written communication skills.
• Excellent task management and organizational skills.
• Ability to multi-task in an always evolving fast paced environment.
• Proficient knowledge of operating common office equipment and software.
• Ability to be ambulatory most of the workday.
• Ability to lift/transfer/push/manipulate equipment and patients.

Responsibilities

• Prioritize tasks and meet deadlines in a fast-paced clinic setting.
• Monitor & report adverse events, protocol deviations, and safety concerns per regulatory guidelines.
• Maintain accurate, audit-ready documentation of all study activities.
• Assist in specimen labeling, storage, and shipment per protocol.
• Establish and maintain patient rapport during clinical trials.
• Coordinate study visits and prepare essential materials (screening packets, informed consents).
• Develop rapport with study sponsors, monitors, and participants.

Skills

Medical office experience

Phlebotomy

Attention to detail

Communication skills

Organization

Multi-tasking

Office software

Ambulatory work

Lifting / assisting patients

Job description

Alliance for Multispecialty Research LLC in Tempe, AZ is seeking a Research Assistant to perform a wide range of administrative and clinical tasks to support study sites. You will assist with protocol adherence, data collection, patient interactions, and study logistics to ensure accurate study execution and audit readiness.

The role emphasizes compliance with GCP, FDA regulations, and sponsor requirements, with potential weekend/overtime hours as needed to support study activities.