Clinical Research Coordinator - Multi-Site Trials & Care

Accel Research Sites; Gilbert (AZ); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Health insurance

401k plan with safe harbor match

Job summary

Accel Research Sites is seeking a Clinical Research Coordinator to join our Operations team at Phoenix Medical Trials in Gilbert, AZ. The CRC will ensure compliant execution of studies across multiple sites, including patient screening, consent, visits, data entry, and safety reporting.

Qualifications include at least 1 year in clinical research or clinical settings, a Medical Assistant diploma or equivalent, and strong organizational and communication skills.

Qualifications

• Minimum 1 year of clinical research or clinical experience required.
• Medical Assistant diploma, LPN/LVN, EMT credential, or Associate’s degree required.
• Bi-lingual English/Spanish proficiency is a plus.

Responsibilities

• Screen patients for study enrollment.
• Obtain patient consents and support follow-up visits.
• Document in source charts and enter data in EDC.
• Obtain vitals, ECGs and basic lab procedures as per protocol.
• Manage study supplies, logs, and file maintenance.
• Coordinate scheduling and patient recruitment as needed.

Skills

MS Office

Clinical procedures

Multitasking

Communication skills

Interpersonal skills

HIPAA compliance

Education

Medical Assistant diploma

LPN/LVN credential

EMT credential

Associate’s degree

Job description

Accel Research Sites is seeking a Clinical Research Coordinator to join our Operations team at Phoenix Medical Trials in Gilbert, AZ. The CRC will ensure compliant execution of studies across multiple sites, including patient screening, consent, visits, data entry, and safety reporting.

Qualifications include at least 1 year in clinical research or clinical settings, a Medical Assistant diploma or equivalent, and strong organizational and communication skills.