Clinical Research Coordinator: Impactful Trials & Care

Alcanza Clinical Research, LLC; Farmington Hills (MI); On-site; USD 52,000 - 70,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

401k plan

Job summary

Alcanza Clinical Research, LLC is seeking a Clinical Research Coordinator (CRC) to ensure the conduct of assigned studies in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs. Located in Farmington Hills, MI, the role operates within the Operations department.

The CRC will screen patients, obtain consents, schedule visits, and document data in EDC, while collecting vital signs, ECGs, and basic lab samples as required. Bilingual English/Spanish is a plus.

Qualifications

• Minimum 1 year of clinical research or clinical experience.
• Proficiency with basic clinical procedures (BP, vitals, EKGs, phlebotomy).
• Bi-lingual English/Spanish is a plus.

Responsibilities

• Screen patients for study enrollment and obtain consent.
• Schedule visits and reminders; document in source charts.
• Enter data in EDC and manage study queries.
• Take vital signs and ECGs; collect lab specimens as needed.
• Maintain logs, supplies, and study documents.

Skills

Medical Assistant diploma

LPN/LVN credential

EMT credential

Associate’s degree

Education

Medical Assistant diploma

LPN/LVN

EMT credential

Associate’s degree

Tools

Electronic Health Records (EHR)

EDC data entry

MS Office

Job description

Alcanza Clinical Research, LLC is seeking a Clinical Research Coordinator (CRC) to ensure the conduct of assigned studies in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs. Located in Farmington Hills, MI, the role operates within the Operations department.

The CRC will screen patients, obtain consents, schedule visits, and document data in EDC, while collecting vital signs, ECGs, and basic lab samples as required. Bilingual English/Spanish is a plus.