Multi-Site Clinical Research Coordinator - Impactful Trials

ActivMed Practices & Research, LLC.; Memphis (IN); On-site; USD 42,000 - 62,000; Full time

Benefits offered by this job

Healthcare benefits

401k with match

HSA

Job summary

Alcanza Clinical Research is seeking a Clinical Research Coordinator to ensure study execution across multiple sites in accordance with GCP, ICH, HIPAA and FDA regulations. You will collaborate with site teams to screen patients, obtain consents, collect data, and help manage study documentation.

The role requires a Medical Assistant diploma or nursing credential and at least one year of clinical research or clinical experience; bilingual English/Spanish is a plus.

Qualifications

• Medical Assistant diploma or related nursing credential plus 1 year of clinical research/clinical experience is required.
• Proficiency with basic clinical procedures (blood pressure, vitals, EKGs, phlebotomy) preferred.
• Bi-lingual English/Spanish proficiency is a plus.

Responsibilities

• Screening patients for study enrollment and obtaining consents.
• Documenting in source charts and entering data in EDC; answering queries.
• Collecting vitals and ECGs; performing basic lab procedures per protocol.

Skills

Microsoft Office

EHR systems

Clinical data entry

Vital signs / ECG

Bi-lingual English/Spanish

Education

Medical Assistant diploma

LPN/LVN

EMT credential

Associate’s degree with clinical research experience

Tools

Electronic data capture (EDC)

ISF document management

HIPAA compliance software

Job description

Alcanza Clinical Research is seeking a Clinical Research Coordinator to ensure study execution across multiple sites in accordance with GCP, ICH, HIPAA and FDA regulations. You will collaborate with site teams to screen patients, obtain consents, collect data, and help manage study documentation.

The role requires a Medical Assistant diploma or nursing credential and at least one year of clinical research or clinical experience; bilingual English/Spanish is a plus.