Multisite Travel Clinical Research Coordinator

Accel Research Sites; Florida; On-site; USD 45,000 - 70,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Short and long-term disability

Health savings account

401k plan with match

Job summary

Alcanza is seeking a Clinical Research Coordinator to support multi-site trials across Phase I‑IV in compliance with GCP, ICH, HIPAA and FDA SOPs. The CRC will screen patients, obtain consents, coordinate visits and document in source charts while traveling to study sites.

Ideal candidates hold a Medical Assistant diploma or LPN/EMT or an Associate degree with 1 year clinical research experience; strong communication and organizational skills are essential; bilingual English/Spanish is a plus.

Qualifications

• A Medical Assistant diploma or equivalent and at least 1 year of clinical research or clinical experience required.
• Proficient in basic clinical procedures: blood pressure, vitals, EKGs, phlebotomy.
• Bi-lingual English/Spanish is a plus.
• Strong organizational, written and verbal communication skills; detail oriented.

Responsibilities

• Screen patients for study enrollment and obtain consents.
• Document in source charts and enter data in EDC.
• Obtain vital signs, ECGs and basic lab procedures as per protocol.
• Schedule visits, reminders and maintain study logs.
• Maintain confidentiality and ensure HIPAA compliance.

Skills

Clinical procedures

Bi-lingual English/Spanish

Organizational skills

Communication skills

HIPAA compliance

Multitasking

Professionalism

Privacy & confidentiality

Typing 40+ wpm

Microsoft Office

Electronic Health Records (EHR)

Education

Medical Assistant diploma

LPN/LVN credential

EMT credential

Associate’s degree

Tools

Microsoft Office

Email client

Electronic Health Records (EHR)

Job description

Alcanza is seeking a Clinical Research Coordinator to support multi-site trials across Phase I‑IV in compliance with GCP, ICH, HIPAA and FDA SOPs. The CRC will screen patients, obtain consents, coordinate visits and document in source charts while traveling to study sites.

Ideal candidates hold a Medical Assistant diploma or LPN/EMT or an Associate degree with 1 year clinical research experience; strong communication and organizational skills are essential; bilingual English/Spanish is a plus.