Clinical Research Coordinator — Multisite Trials & Impact

Accel Research Sites; Farmington Hills (MI); On-site; USD 52,000 - 68,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401k plan with safe harbor match

Health savings accounts

Job summary

Alcanza is seeking a Clinical Research Coordinator to join our Operations team at Quest Research Institute in Farmington Hills, MI. The CRC will ensure study execution in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs.

Responsibilities include patient screening, consent, follow-up visits, data entry, vital signs/ECGs, sample handling, and coordination of study activities. Strong clinical procedures experience and bilingual ability are a plus.

Qualifications

• Medical Assistant diploma, LPN/LVN, EMT credential or Associate’s degree with 1 year clinical research/clinical experience.
• Proficiency performing basic clinical procedures (BP, vitals, EKGs, phlebotomy).
• Bi-lingual English/Spanish is a plus.
• Proficient with Microsoft Office, EHRs and 40+ wpm typing.
• Strong organizational and communication skills.

Responsibilities

• Screen patients for study enrollment.
• Obtain patient consents and schedule follow-up visits.
• Document in source clinic charts; enter data in EDC and answer queries.
• Obtain vital signs and ECGs; perform basic lab procedures per protocol.
• Maintain logs and study-specific supplies; coordinate with team and sponsors.
• Ensure confidentiality and HIPAA compliance in all activities.
• Assist with recruitment and tracking as needed.

Skills

Clinical procedures

Microsoft Office

EHR systems

Communication skills

Bilingual English/Spanish

Organization

Education

Medical Assistant diploma/LPN/LVN/EMT credential OR Associate degree

1 year clinical research/clinical experience

Job description

Alcanza is seeking a Clinical Research Coordinator to join our Operations team at Quest Research Institute in Farmington Hills, MI. The CRC will ensure study execution in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs.

Responsibilities include patient screening, consent, follow-up visits, data entry, vital signs/ECGs, sample handling, and coordination of study activities. Strong clinical procedures experience and bilingual ability are a plus.