Clinical Research Coordinator - Multi-Site Trials & Patient Care

ActivMed Practices & Research, LLC.; Farmington Hills (MI); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

401k with safe harbor match

Job summary

Alcanza Clinical Research is seeking a Clinical Research Coordinator (CRC) to join our multi-site network. You will ensure study execution in alignment with GCP, ICH, HIPAA, FDA regulations, and SOPs, collaborating with the site team.

Responsibilities include screening patients, obtaining consents, coordinating visits, entering data, collecting vital signs and ECGs, and maintaining study documentation. A background in clinical research and bilingual skills are strong pluses.

Qualifications

• Medical Assistant diploma, LPN/LVN, EMT credential or Associate’s degree with 1 year clinical research/clinical experience.
• Proficiency in basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy.
• Bi-lingual English/Spanish proficiency is a plus.

Responsibilities

• Screen patients for study enrollment and obtain informed consent.
• Perform patient visits, collect data and vitals, and record information.
• Maintain study logs, source documentation, and regulatory filings.
• Assist with study recruitment and ensure HIPAA compliance.

Skills

Clinical research experience

Basic clinical procedures

Bilingual English/Spanish

Organizational skills

Communication skills

Independent work

HIPAA compliance

Education

Medical Assistant diploma

LPN/LVN credential

EMT credential

Associate’s degree

Tools

Electronic health records

Job description

Alcanza Clinical Research is seeking a Clinical Research Coordinator (CRC) to join our multi-site network. You will ensure study execution in alignment with GCP, ICH, HIPAA, FDA regulations, and SOPs, collaborating with the site team.

Responsibilities include screening patients, obtaining consents, coordinating visits, entering data, collecting vital signs and ECGs, and maintaining study documentation. A background in clinical research and bilingual skills are strong pluses.